LABELS · f4c6a69e-cc09-4328-a863-8c32a7f73a68
Solu-Medrol
Open original source → · Download preserved record
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
- 2026-03-18
- Captured
- 2026-09-09T23:38:04.335995+00:00
- Current indication reconciliation
- Not reconciled
Indications and usage: exact source 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-MEDROL 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, exfoliiative 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, nonsupportable thyroiditis. Gastrointestinal diseases: To tide the patient over a critical period of the disease in regional enteritis (systemic therapy) and ulcerative colitis. Hemotologic 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, selected 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 adema 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
- NDA011856
- boxed warning exact
- brand names
- Solu-Medrol
- current indication status
- not_reconciled
- dailymed set url
- https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=decceb81-e922-4b72-a278-3ed80f4adb04
- generic names
- METHYLPREDNISOLONE SODIUM SUCCINATE
- id
- f4c6a69e-cc09-4328-a863-8c32a7f73a68
- indications and usage exact
- 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-MEDROL 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, exfoliiative 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, nonsupportable thyroiditis. Gastrointestinal diseases: To tide the patient over a critical period of the disease in regional enteritis (systemic therapy) and ulcerative colitis. Hemotologic 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, selected 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 adema 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
- Henry Schein, Inc.
- matched search terms
- cancer
- lymphomas
- tumor
- package ndcs
- 0404-9958-01
- product ndcs
- 0404-9958
- product types
- HUMAN PRESCRIPTION DRUG
- recent major changes exact
- record type
- complete_spl_indications_section_candidate
- routes
- INTRAMUSCULAR
- INTRAVENOUS
- rxcuis
- 207191
- 311659
- source batch
- file
- /private/tmp/cancer-full-research/indications/raw/labels-00800.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
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Drugs@FDA application source records
- application number
- NDA011856
- payload
- all indexed label documents
- Appl No
- 011856
- Application Docs Date
- 2011-10-25 00:00:00
- Application Docs ID
- 10784
- Application Docs Title
- 0
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- 2
- Application Docs URL
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- 104
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- 107
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- 011856
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- 123
- Submission Type
- SUPPL
- Appl No
- 011856
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- 0
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- 2
- Application Docs URL
- http://www.accessdata.fda.gov/drugsatfda_docs/label/2016/011856s124and126lbl.pdf
- Submission No
- 124
- Submission Type
- SUPPL
- Appl No
- 011856
- Application Docs Date
- 2016-09-09 00:00:00
- Application Docs ID
- 45263
- Application Docs Title
- 0
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- 2
- Application Docs URL
- http://www.accessdata.fda.gov/drugsatfda_docs/label/2016/011856s124and126lbl.pdf
- Submission No
- 126
- Submission Type
- SUPPL
- Appl No
- 011856
- Application Docs Date
- 2018-04-01 00:00:00
- Application Docs ID
- 53571
- Application Docs Title
- 0
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- 2
- Application Docs URL
- https://www.accessdata.fda.gov/drugsatfda_docs/label/2018/011856s131lbl.pdf
- Submission No
- 131
- Submission Type
- SUPPL
- Appl No
- 011856
- Application Docs Date
- 2018-07-25 00:00:00
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- 54963
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- 0
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- Application Docs URL
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- Submission No
- 133
- Submission Type
- SUPPL
- Appl No
- 011856
- Application Docs Date
- 2021-06-04 00:00:00
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- 0
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- 2
- Application Docs URL
- http://www.accessdata.fda.gov/drugsatfda_docs/label/2021/011856s136lbl.pdf
- Submission No
- 136
- Submission Type
- SUPPL
- Appl No
- 011856
- Application Docs Date
- 2021-11-29 00:00:00
- Application Docs ID
- 69419
- Application Docs Title
- 0
- Application Docs Type ID
- 2
- Application Docs URL
- http://www.accessdata.fda.gov/drugsatfda_docs/label/2021/011856s139lbl.pdf
- Submission No
- 139
- Submission Type
- SUPPL
- Appl No
- 011856
- Application Docs Date
- 2023-12-21 00:00:00
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- 77105
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- 0
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- 2
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- http://www.accessdata.fda.gov/drugsatfda_docs/label/2023/011856s141lbl.pdf
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- 011856
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- 2024-06-06 00:00:00
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- 0
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- Appl No
- 011856
- Review Priority
- STANDARD
- Submission Class Code ID
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- Submission No
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- Appl No
- 011856
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- Appl No
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- Appl No
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- approval interpretation
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- current indication status
- not_reconciled
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- has approved submission record
- true
- latest approved submission date
- 2025-11-04
- 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
- Appl No
- 011856
- Application Docs Date
- 2025-11-07 00:00:00
- Application Docs ID
- 84121
- Application Docs Title
- 0
- Application Docs Type ID
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- Application Docs URL
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- official application record
- Appl No
- 011856
- Appl Public Notes
- Appl Type
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- Sponsor Name
- PHARMACIA AND UPJOHN
- openfda application present
- true
- products
- Active Ingredient
- METHYLPREDNISOLONE SODIUM SUCCINATE
- Appl No
- 011856
- Drug Name
- SOLU-MEDROL
- Form
- INJECTABLE;INJECTION
- Product No
- 003
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- 1
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- EQ 40MG BASE/VIAL
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- METHYLPREDNISOLONE SODIUM SUCCINATE
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- Appl No
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- METHYLPREDNISOLONE SODIUM SUCCINATE
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- Appl No
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- Product No
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- Reference Drug
- 1
- Reference Standard
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- Strength
- EQ 2GM BASE/VIAL
- marketing status
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Source passages and status connections
Passage 1 · positive indication candidate
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- 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-MEDROL 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, exfoliiative erythroderma, mycosis fungoides, pemphigus, severe erythema multiforme (Stevens-Johnson syndrome). Endocrine disorders: Primary o
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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-MEDROL 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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Passage 2 · unclassified context
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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, exfoliiative 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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Passage 3 · unclassified context
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Passage 5 · risk or warning
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Passage 6 · unclassified context
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Passage 7 · unclassified context
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Passage 8 · unclassified context
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Passage 9 · unclassified context
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Passage 10 · unclassified context
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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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- use intent
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Passage 11 · unclassified context
- application numbers
- NDA011856
- brand names
- Solu-Medrol
- classification reasons
- no_unambiguous_positive_indication_predicate
- clinical review status
- pending
- content role
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- ar 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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- Respiratory diseases: Berylliosis, fulminating or disseminated pulmonary tuberculosis when used concurrently with appropriate antituberculous chemotherapy, idiopathic eosinophilic pneumonias, symptomatic sarcoidosis.
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- limitations
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- Source null
- regimen
- Source null
- tumor histology
- Source null
- use intent
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Passage 12 · unclassified context
- application numbers
- NDA011856
- brand names
- Solu-Medrol
- classification reasons
- no_unambiguous_positive_indication_predicate
- clinical review status
- pending
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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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- 2276
- current approval status
- not_reconciled
- duplicate text group
- dup-7cad36e1b047df4bbc7a
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- generic names
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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
- 2476
- source url
- https://api.fda.gov/drug/label.json?search=id%3A%22f4c6a69e-cc09-4328-a863-8c32a7f73a68%22
- spl effective date
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- Source null
- limitations
- Source null
- line
- Source null
- prior therapy
- Source null
- regimen
- Source null
- tumor histology
- Source null
- use intent
- unclear
Passage 13 · unclassified context
- application numbers
- NDA011856
- brand names
- Solu-Medrol
- classification reasons
- no_unambiguous_positive_indication_predicate
- clinical review status
- pending
- content role
- unclassified_context
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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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- start
- 2627
- current approval status
- not_reconciled
- duplicate text group
- dup-c2d36851a742917232ba
- extraction review status
- automated_candidate_pending_source_review
- generic names
- METHYLPREDNISOLONE SODIUM SUCCINATE
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- ind-span-9fc07975d42407330b6d
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- exact text
- For the treatment of dermatomyositis, temporal arteritis, polymyositis, and systemic lupus erythematosus.
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- start
- 2827
- source url
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- spl effective date
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- structured fields status
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- structured indication
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- limitations
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- line
- Source null
- prior therapy
- Source null
- regimen
- Source null
- tumor histology
- Source null
- use intent
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Preserved source evidence · Not medical advice
Triangle