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LABELS · 4e9814fe-3089-4980-a207-bf0aa95d4c36

Solu-Cortef

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Preserved label snapshot, not confirmation of a current approved indication. Approval/withdrawal status must be checked for the exact disease, setting and regimen.

Label effective date
2026-08-27
Captured
2026-09-09T23:37:47.659725+00:00
Current indication reconciliation
Not reconciled

Indications and usage: exact source text

  1. INDICATIONS AND USAGE When oral therapy is not feasible, and the strength, dosage form, and route of administration of the drug reasonably lend the preparation to the treatment of the condition, the intravenous or intramuscular use of SOLU-CORTEF Sterile Powder is indicated as follows: Allergic states: Control of severe or incapacitating allergic conditions intractable to adequate trials of conventional treatment in asthma, atopic dermatitis, contact dermatitis, drug hypersensitivity reactions, serum sickness, transfusion reactions. Dermatologic diseases: Bullous dermatitis herpetiformis, exfoliative erythroderma, mycosis fungoides, pemphigus, severe erythema multiforme (Stevens-Johnson syndrome). Endocrine disorders: Primary or secondary adrenocortical insufficiency (hydrocortisone or cortisone is the drug of choice; synthetic analogs may be used in conjunction with mineralocorticoids where applicable; in infancy, mineralocorticoid supplementation is of particular importance), congenital adrenal hyperplasia, hypercalcemia associated with cancer, nonsuppurative thyroiditis. Gastrointestinal diseases: To tide the patient over a critical period of the disease in regional enteritis (systemic therapy) and ulcerative colitis. Hematologic disorders: Acquired (autoimmune) hemolytic anemia, congenital (erythroid) hypoplastic anemia (Diamond Blackfan anemia), idiopathic thrombocytopenic purpura in adults (intravenous administration only; intramuscular administration is contraindicated), pure red cell aplasia, select cases of secondary thrombocytopenia. Miscellaneous: Trichinosis with neurologic or myocardial involvement, tuberculous meningitis with subarachnoid block or impending block when used concurrently with appropriate antituberculous chemotherapy. Neoplastic diseases: For the palliative management of leukemias and lymphomas. Nervous System: Cerebral edema associated with primary or metastatic brain tumor, or craniotomy. Ophthalmic diseases: Sympathetic ophthalmia, uveitis and ocular inflammatory conditions unresponsive to topical corticosteroids. Renal diseases: To induce diuresis or remission of proteinuria in idiopathic nephrotic syndrome, or that due to lupus erythematosus. Respiratory diseases: Berylliosis, fulminating or disseminated pulmonary tuberculosis when used concurrently with appropriate antituberculous chemotherapy, idiopathic eosinophilic pneumonias, symptomatic sarcoidosis. Rheumatic disorders: As adjunctive therapy for short-term administration (to tide the patient over an acute episode or exacerbation) in acute gouty arthritis; acute rheumatic carditis; ankylosing spondylitis; psoriatic arthritis; rheumatoid arthritis, including juvenile rheumatoid arthritis (selected cases may require low-dose maintenance therapy). For the treatment of dermatomyositis, temporal arteritis, polymyositis, and systemic lupus erythematosus.
Full extracted label fields
application numbers
  1. NDA009866
boxed warning exact
    brand names
    1. Solu-Cortef
    current indication status
    not_reconciled
    dailymed set url
    https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=65eefd58-b166-4d71-ade6-45c8fdf86922
    generic names
    1. HYDROCORTISONE SODIUM SUCCINATE
    id
    4e9814fe-3089-4980-a207-bf0aa95d4c36
    indications and usage exact
    1. INDICATIONS AND USAGE When oral therapy is not feasible, and the strength, dosage form, and route of administration of the drug reasonably lend the preparation to the treatment of the condition, the intravenous or intramuscular use of SOLU-CORTEF Sterile Powder is indicated as follows: Allergic states: Control of severe or incapacitating allergic conditions intractable to adequate trials of conventional treatment in asthma, atopic dermatitis, contact dermatitis, drug hypersensitivity reactions, serum sickness, transfusion reactions. Dermatologic diseases: Bullous dermatitis herpetiformis, exfoliative erythroderma, mycosis fungoides, pemphigus, severe erythema multiforme (Stevens-Johnson syndrome). Endocrine disorders: Primary or secondary adrenocortical insufficiency (hydrocortisone or cortisone is the drug of choice; synthetic analogs may be used in conjunction with mineralocorticoids where applicable; in infancy, mineralocorticoid supplementation is of particular importance), congenital adrenal hyperplasia, hypercalcemia associated with cancer, nonsuppurative thyroiditis. Gastrointestinal diseases: To tide the patient over a critical period of the disease in regional enteritis (systemic therapy) and ulcerative colitis. Hematologic disorders: Acquired (autoimmune) hemolytic anemia, congenital (erythroid) hypoplastic anemia (Diamond Blackfan anemia), idiopathic thrombocytopenic purpura in adults (intravenous administration only; intramuscular administration is contraindicated), pure red cell aplasia, select cases of secondary thrombocytopenia. Miscellaneous: Trichinosis with neurologic or myocardial involvement, tuberculous meningitis with subarachnoid block or impending block when used concurrently with appropriate antituberculous chemotherapy. Neoplastic diseases: For the palliative management of leukemias and lymphomas. Nervous System: Cerebral edema associated with primary or metastatic brain tumor, or craniotomy. Ophthalmic diseases: Sympathetic ophthalmia, uveitis and ocular inflammatory conditions unresponsive to topical corticosteroids. Renal diseases: To induce diuresis or remission of proteinuria in idiopathic nephrotic syndrome, or that due to lupus erythematosus. Respiratory diseases: Berylliosis, fulminating or disseminated pulmonary tuberculosis when used concurrently with appropriate antituberculous chemotherapy, idiopathic eosinophilic pneumonias, symptomatic sarcoidosis. Rheumatic disorders: As adjunctive therapy for short-term administration (to tide the patient over an acute episode or exacerbation) in acute gouty arthritis; acute rheumatic carditis; ankylosing spondylitis; psoriatic arthritis; rheumatoid arthritis, including juvenile rheumatoid arthritis (selected cases may require low-dose maintenance therapy). For the treatment of dermatomyositis, temporal arteritis, polymyositis, and systemic lupus erythematosus.
    indications and usage tables exact
      is original packager
      1. true
      manufacturer names
      1. Pharmacia & Upjohn Company LLC
      matched search terms
      1. cancer
      2. lymphomas
      3. tumor
      package ndcs
      1. 0009-0825-01
      2. 0009-0011-03
      3. 0009-0011-04
      4. 0009-0013-05
      5. 0009-0013-06
      6. 0009-0016-12
      7. 0009-0005-01
      product ndcs
      1. 0009-0005
      2. 0009-0825
      3. 0009-0011
      4. 0009-0013
      5. 0009-0016
      product types
      1. HUMAN PRESCRIPTION DRUG
      recent major changes exact
        record type
        complete_spl_indications_section_candidate
        routes
        1. INTRAMUSCULAR
        2. INTRAVENOUS
        rxcuis
        1. 105398
        2. 238755
        3. 1738586
        4. 1738589
        5. 1738590
        6. 1738592
        7. 1738594
        8. 1738596
        source batch
        file
        /private/tmp/cancer-full-research/indications/raw/labels-00300.json
        meta
        disclaimer
        Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. We may limit or otherwise restrict your access to the API in line with our Terms of Service.
        last updated
        2026-09-09
        results
        limit
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        skip
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        total
        830
        sha256
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        url
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        source url
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        spl effective date
        2026-08-27
        spl effective time
        20260827
        spl set id
        65eefd58-b166-4d71-ade6-45c8fdf86922
        spl version
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        substance names
        1. HYDROCORTISONE SODIUM SUCCINATE
        uniis
        1. 50LQB69S1Z
        verification flags
        1. oncology_keyword_candidate_not_clinically_classified
        2. spl_text_not_verified_identical_to_latest_approved_label
        3. individual_indications_not_split_or_reconciled
        Drugs@FDA application source records
        1. application number
          NDA009866
          payload
          all indexed label documents
          1. Appl No
            009866
            Application Docs Date
            2009-10-05 00:00:00
            Application Docs ID
            10733
            Application Docs Title
            0
            Application Docs Type ID
            2
            Submission No
            79
            Submission Type
            SUPPL
          2. Appl No
            009866
            Application Docs Date
            2010-07-01 00:00:00
            Application Docs ID
            10734
            Application Docs Title
            0
            Application Docs Type ID
            2
            Submission No
            80
            Submission Type
            SUPPL
          3. Appl No
            009866
            Application Docs Date
            2009-10-05 00:00:00
            Application Docs ID
            33007
            Application Docs Title
            0
            Application Docs Type ID
            2
            Submission No
            77
            Submission Type
            SUPPL
          4. Appl No
            009866
            Application Docs Date
            2014-07-08 00:00:00
            Application Docs ID
            33008
            Application Docs Title
            0
            Application Docs Type ID
            2
            Submission No
            104
            Submission Type
            SUPPL
          5. Appl No
            009866
            Application Docs Date
            2016-09-09 00:00:00
            Application Docs ID
            45259
            Application Docs Title
            0
            Application Docs Type ID
            2
            Submission No
            98
            Submission Type
            SUPPL
          6. Appl No
            009866
            Application Docs Date
            2016-09-09 00:00:00
            Application Docs ID
            45260
            Application Docs Title
            0
            Application Docs Type ID
            2
            Submission No
            105
            Submission Type
            SUPPL
          7. Appl No
            009866
            Application Docs Date
            2019-11-22 00:00:00
            Application Docs ID
            61014
            Application Docs Title
            0
            Application Docs Type ID
            2
            Submission No
            113
            Submission Type
            SUPPL
          8. Appl No
            009866
            Application Docs Date
            2021-06-04 00:00:00
            Application Docs ID
            67698
            Application Docs Title
            0
            Application Docs Type ID
            2
            Submission No
            115
            Submission Type
            SUPPL
          9. Appl No
            009866
            Application Docs Date
            2023-12-21 00:00:00
            Application Docs ID
            77103
            Application Docs Title
            0
            Application Docs Type ID
            2
            Submission No
            119
            Submission Type
            SUPPL
          10. Appl No
            009866
            Application Docs Date
            2024-06-06 00:00:00
            Application Docs ID
            78671
            Application Docs Title
            0
            Application Docs Type ID
            2
            Submission No
            121
            Submission Type
            SUPPL
          11. Appl No
            009866
            Application Docs Date
            2024-07-18 00:00:00
            Application Docs ID
            79122
            Application Docs Title
            0
            Application Docs Type ID
            2
            Submission No
            120
            Submission Type
            SUPPL
          all submission records
          1. Appl No
            009866
            Review Priority
            STANDARD
            Submission Class Code ID
            3
            Submission No
            121
            Submission Status
            AP
            Submission Status Date
            2024-06-05 00:00:00
            Submission Type
            SUPPL
            Submissions Public Notes
          2. Appl No
            009866
            Review Priority
            STANDARD
            Submission Class Code ID
            3
            Submission No
            120
            Submission Status
            AP
            Submission Status Date
            2024-07-10 00:00:00
            Submission Type
            SUPPL
            Submissions Public Notes
          3. Appl No
            009866
            Review Priority
            STANDARD
            Submission Class Code ID
            3
            Submission No
            119
            Submission Status
            AP
            Submission Status Date
            2023-12-20 00:00:00
            Submission Type
            SUPPL
            Submissions Public Notes
          4. Appl No
            009866
            Review Priority
            STANDARD
            Submission Class Code ID
            3
            Submission No
            115
            Submission Status
            AP
            Submission Status Date
            2021-05-27 00:00:00
            Submission Type
            SUPPL
            Submissions Public Notes
          5. Appl No
            009866
            Review Priority
            STANDARD
            Submission Class Code ID
            3
            Submission No
            113
            Submission Status
            AP
            Submission Status Date
            2019-11-21 00:00:00
            Submission Type
            SUPPL
            Submissions Public Notes
          6. Appl No
            009866
            Review Priority
            STANDARD
            Submission Class Code ID
            4
            Submission No
            108
            Submission Status
            AP
            Submission Status Date
            2016-02-25 00:00:00
            Submission Type
            SUPPL
            Submissions Public Notes
          7. Appl No
            009866
            Review Priority
            STANDARD
            Submission Class Code ID
            3
            Submission No
            105
            Submission Status
            AP
            Submission Status Date
            2016-09-08 00:00:00
            Submission Type
            SUPPL
            Submissions Public Notes
          8. Appl No
            009866
            Review Priority
            STANDARD
            Submission Class Code ID
            3
            Submission No
            104
            Submission Status
            AP
            Submission Status Date
            2014-07-03 00:00:00
            Submission Type
            SUPPL
            Submissions Public Notes
          9. Appl No
            009866
            Review Priority
            STANDARD
            Submission Class Code ID
            4
            Submission No
            103
            Submission Status
            AP
            Submission Status Date
            2014-06-24 00:00:00
            Submission Type
            SUPPL
            Submissions Public Notes
          10. Appl No
            009866
            Review Priority
            STANDARD
            Submission Class Code ID
            4
            Submission No
            102
            Submission Status
            AP
            Submission Status Date
            2014-06-09 00:00:00
            Submission Type
            SUPPL
            Submissions Public Notes
          11. Appl No
            009866
            Review Priority
            STANDARD
            Submission Class Code ID
            4
            Submission No
            101
            Submission Status
            AP
            Submission Status Date
            2014-07-22 00:00:00
            Submission Type
            SUPPL
            Submissions Public Notes
          12. Appl No
            009866
            Review Priority
            STANDARD
            Submission Class Code ID
            4
            Submission No
            99
            Submission Status
            AP
            Submission Status Date
            2014-03-28 00:00:00
            Submission Type
            SUPPL
            Submissions Public Notes
          application number
          NDA009866
          approval interpretation
          Application linkage and approved submission are not indication-level current approval verification
          current indication status
          not_reconciled
          has approved submission record
          true
          latest approved submission date
          2024-07-10
          latest label selection rule
          max FDA ApplicationDocsDate, including all ties; posting date is not approval date and latest indexed document may be incomplete
          latest posted label documents
          1. Appl No
            009866
            Application Docs Date
            2024-07-18 00:00:00
            Application Docs ID
            79122
            Application Docs Title
            0
            Application Docs Type ID
            2
            Submission No
            120
            Submission Type
            SUPPL
          official application record
          Appl No
          009866
          Appl Public Notes
          Appl Type
          NDA
          Sponsor Name
          PHARMACIA AND UPJOHN
          openfda application present
          true
          products
          1. Active Ingredient
            HYDROCORTISONE SODIUM SUCCINATE
            Appl No
            009866
            Drug Name
            SOLU-CORTEF
            Form
            INJECTABLE;INJECTION
            Product No
            001
            Reference Drug
            1
            Reference Standard
            1
            Strength
            EQ 100MG BASE/VIAL
            marketing status
            1. Prescription
          2. Active Ingredient
            HYDROCORTISONE SODIUM SUCCINATE
            Appl No
            009866
            Drug Name
            SOLU-CORTEF
            Form
            INJECTABLE;INJECTION
            Product No
            002
            Reference Drug
            1
            Reference Standard
            1
            Strength
            EQ 250MG BASE/VIAL
            marketing status
            1. Prescription
          3. Active Ingredient
            HYDROCORTISONE SODIUM SUCCINATE
            Appl No
            009866
            Drug Name
            SOLU-CORTEF
            Form
            INJECTABLE;INJECTION
            Product No
            003
            Reference Drug
            1
            Reference Standard
            1
            Strength
            EQ 500MG BASE/VIAL
            marketing status
            1. Prescription
          4. Active Ingredient
            HYDROCORTISONE SODIUM SUCCINATE
            Appl No
            009866
            Drug Name
            SOLU-CORTEF
            Form
            INJECTABLE;INJECTION
            Product No
            004
            Reference Drug
            1
            Reference Standard
            1
            Strength
            EQ 1GM BASE/VIAL
            marketing status
            1. Prescription

        Source passages and status connections

        Passage classifications are automated and are not treatment recommendations. Connections apply only to their recorded indication scope.

        Passage 1 · positive indication candidate
        application numbers
        1. NDA009866
        brand names
        1. Solu-Cortef
        classification reasons
        1. explicit_positive_indication_predicate
        2. no_tumor_directed_keyword_in_positive_statement
        clinical review status
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        true
        exact text
        INDICATIONS AND USAGE When oral therapy is not feasible, and the strength, dosage form, and route of administration of the drug reasonably lend the preparation to the treatment of the condition, the intravenous or intramuscular use of SOLU-CORTEF Sterile Powder is indicated as follows: Allergic states: Control of severe or incapacitating allergic conditions intractable to adequate trials of conventional treatment in asthma, atopic dermatitis, contact dermatitis, drug hypersensitivity reactions, serum sickness, transfusion reactions. Dermatologic diseases: Bullous dermatitis herpetiformis, exfoliative erythroderma, mycosis fungoides, pemphigus, severe erythema multiforme (Stevens-Johnson syndrome). Endocrine disorders: Primary or
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              INDICATIONS AND USAGE When oral therapy is not feasible, and the strength, dosage form, and route of administration of the drug reasonably lend the preparation to the treatment of the condition, the intravenous or intramuscular use of SOLU-CORTEF Sterile Powder is indicated as follows: Allergic states: Control of severe or incapacitating allergic conditions intractable to adequate trials of conventional treatment in asthma, atopic dermatitis, contact dermatitis, drug hypersensitivity reactions, serum sickness, transfusion reactions.
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              Source null
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              Source null
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              Source null
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              Source null
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              Source null
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              Source null
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              Source null
              regimen
              Source null
              tumor histology
              Source null
              use intent
              non_oncology_or_unclear_candidate
              Passage 2 · unclassified context
              application numbers
              1. NDA009866
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              allergic conditions intractable to adequate trials of conventional treatment in asthma, atopic dermatitis, contact dermatitis, drug hypersensitivity reactions, serum sickness, transfusion reactions. Dermatologic diseases: Bullous dermatitis herpetiformis, exfoliative erythroderma, mycosis fungoides, pemphigus, severe erythema multiforme (Stevens-Johnson syndrome). Endocrine disorders: Primary or secondary adrenocortical insufficiency (hydrocortisone or cortisone is the drug of choice; synthetic analogs may be used in conjunction with mineralocorticoids where a
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                    Dermatologic diseases: Bullous dermatitis herpetiformis, exfoliative erythroderma, mycosis fungoides, pemphigus, severe erythema multiforme (Stevens-Johnson syndrome).
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                    spl effective date
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                    Source null
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                    Source null
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                    Source null
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                    Source null
                    limitations
                    Source null
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                    Source null
                    prior therapy
                    Source null
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                                                          Ophthalmic diseases: Sympathetic ophthalmia, uveitis and ocular inflammatory conditions unresponsive to topical corticosteroids.
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                                                          start
                                                          1952
                                                          source url
                                                          https://api.fda.gov/drug/label.json?search=id%3A%224e9814fe-3089-4980-a207-bf0aa95d4c36%22
                                                          spl effective date
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                                                          line
                                                          Source null
                                                          prior therapy
                                                          Source null
                                                          regimen
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                                                          use intent
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                                                          Passage 10 · unclassified context
                                                          application numbers
                                                          1. NDA009866
                                                          brand names
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                                                          classification reasons
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                                                          dema associated with primary or metastatic brain tumor, or craniotomy. Ophthalmic diseases: Sympathetic ophthalmia, uveitis and ocular inflammatory conditions unresponsive to topical corticosteroids. Renal diseases: To induce diuresis or remission of proteinuria in idiopathic nephrotic syndrome, or that due to lupus erythematosus. Respiratory diseases: Berylliosis, fulminating or disseminated pulmonary tuberculosis when used concurrently with appropriate antituberculous chemotherapy, idiopathic eosinophilic pneumonias, symptom
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                                                                Renal diseases: To induce diuresis or remission of proteinuria in idiopathic nephrotic syndrome, or that due to lupus erythematosus.
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                                                                Passage 11 · unclassified context
                                                                application numbers
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                                                                classification reasons
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                                                                r inflammatory conditions unresponsive to topical corticosteroids. Renal diseases: To induce diuresis or remission of proteinuria in idiopathic nephrotic syndrome, or that due to lupus erythematosus. Respiratory diseases: Berylliosis, fulminating or disseminated pulmonary tuberculosis when used concurrently with appropriate antituberculous chemotherapy, idiopathic eosinophilic pneumonias, symptomatic sarcoidosis. Rheumatic disorders: As adjunctive therapy for short-term administration (to tide the patient over an acute episode or exacerbation) in acute gouty arthritis; acute rheumatic carditis; ankylosing spo
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                                                                start
                                                                2014
                                                                current approval status
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                                                                duplicate text group
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                                                                      Respiratory diseases: Berylliosis, fulminating or disseminated pulmonary tuberculosis when used concurrently with appropriate antituberculous chemotherapy, idiopathic eosinophilic pneumonias, symptomatic sarcoidosis.
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                                                                      start
                                                                      2214
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                                                                      Passage 12 · unclassified context
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                                                                      ses: Berylliosis, fulminating or disseminated pulmonary tuberculosis when used concurrently with appropriate antituberculous chemotherapy, idiopathic eosinophilic pneumonias, symptomatic sarcoidosis. Rheumatic disorders: As adjunctive therapy for short-term administration (to tide the patient over an acute episode or exacerbation) in acute gouty arthritis; acute rheumatic carditis; ankylosing spondylitis; psoriatic arthritis; rheumatoid arthritis, including juvenile rheumatoid arthritis (selected cases may require low-dose maintenance therapy). For the treatment of dermatomyositis, temporal arteritis, polymyositis, and systemic lupus erythematosus.
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                                                                            Rheumatic disorders: As adjunctive therapy for short-term administration (to tide the patient over an acute episode or exacerbation) in acute gouty arthritis; acute rheumatic carditis; ankylosing spondylitis; psoriatic arthritis; rheumatoid arthritis, including juvenile rheumatoid arthritis (selected cases may require low-dose maintenance therapy).
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                                                                            start
                                                                            2431
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                                                                            Passage 13 · unclassified context
                                                                            application numbers
                                                                            1. NDA009866
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                                                                            classification reasons
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                                                                            hritis; acute rheumatic carditis; ankylosing spondylitis; psoriatic arthritis; rheumatoid arthritis, including juvenile rheumatoid arthritis (selected cases may require low-dose maintenance therapy). For the treatment of dermatomyositis, temporal arteritis, polymyositis, and systemic lupus erythematosus.
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                                                                                  For the treatment of dermatomyositis, temporal arteritis, polymyositis, and systemic lupus erythematosus.
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                                                                                  2782
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                                                                                  Source null
                                                                                  use intent
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                                                                                  Preserved source evidence · Not medical advice