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LABELS · 1203ca7f-080b-4c49-e063-6294a90a90e0

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
2024-02-22
Captured
2026-09-09T23:37:39.774134+00:00
Current indication reconciliation
Not reconciled

Indications and usage: exact source text

  1. INDICATIONS & 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 intramusculat 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, perennial or seasonal allergic rhinitis, 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 Acute exacerbations of multiple sclerosis; 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=74f84173-a43f-7788-e053-2991aa0a8fb2
    generic names
    1. SOLU-CORTEF
    id
    1203ca7f-080b-4c49-e063-6294a90a90e0
    indications and usage exact
    1. INDICATIONS & 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 intramusculat 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, perennial or seasonal allergic rhinitis, 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 Acute exacerbations of multiple sclerosis; 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
        manufacturer names
        1. HF Acquisition Co. LLC, DBA HealthFirst
        matched search terms
        1. cancer
        2. lymphomas
        3. tumor
        package ndcs
        1. 51662-1261-1
        2. 51662-1261-2
        3. 51662-1261-3
        product ndcs
        1. 51662-1261
        product types
        1. HUMAN PRESCRIPTION DRUG
        recent major changes exact
          record type
          complete_spl_indications_section_candidate
          routes
          1. INTRAMUSCULAR
          2. INTRAVENOUS
          rxcuis
          1. 238755
          source batch
          file
          /private/tmp/cancer-full-research/indications/raw/labels-00000.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
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          sha256
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          url
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          source url
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          spl effective date
          2024-02-22
          spl effective time
          20240222
          spl set id
          74f84173-a43f-7788-e053-2991aa0a8fb2
          spl version
          6
          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
          4. not_identified_as_original_packager
          5. fda_label_posted_after_spl_effective_date_requires_version_review
          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
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          clinical review status
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          exact text
          INDICATIONS & 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 intramusculat 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, perennial or seasonal allergic rhinitis, serum sickness, transfusion reactions. Dermatologic diseases Bullous dermatitis herpetiformis, exfoliative erythroderma, mycosis fungoides, pemphigus, severe erythema multiforme (Stevens-Johnson syndrome). Endocrine disorders Primary or s
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                INDICATIONS & 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 intramusculat 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, perennial or seasonal allergic rhinitis, 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
                regimen
                Source null
                tumor histology
                Source null
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                non_oncology_or_unclear_candidate
                Passage 2 · unclassified context
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                ate trials of conventional treatment in asthma, atopic dermatitis, contact dermatitis, drug hypersensitivity reactions, perennial or seasonal allergic rhinitis, 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 ap
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                      Dermatologic diseases Bullous dermatitis herpetiformis, exfoliative erythroderma, mycosis fungoides, pemphigus, severe erythema multiforme (Stevens-Johnson syndrome).
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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
                      regimen
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                      tumor histology
                      Source null
                      use intent
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                      Passage 3 · unclassified context
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                      brand names
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                                                            Ophthalmic diseases Sympathetic ophthalmia, uveitis and ocular inflammatory conditions unresponsive to topical corticosteroids.
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                                                            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, symptoma
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                                                                        ases 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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                                                                                    For the treatment of dermatomyositis, temporal arteritis, polymyositis, and systemic lupus erythematosus.
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                                                                                    Preserved source evidence · Not medical advice