LABELS · 008c23fa-2a90-4621-b5a6-cf9262c9319d
KENALOG-40
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
- 2025-12-05
- Captured
- 2026-09-09T23:37:39.774134+00:00
- Current indication reconciliation
- Not reconciled
Indications and usage: exact source text
- INDICATIONS AND USAGE Intramuscular Where oral therapy is not feasible, injectable corticosteroid therapy, including KENALOG-40 Injection and KENALOG-80 Injection (triamcinolone acetonide injectable suspension, USP) is indicated for intramuscular use 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 and ulcerative colitis. Hematologic disorders: Acquired (autoimmune) hemolytic anemia, Diamond-Blackfan anemia, 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 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, temporal arteritis, 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, polymyositis, and systemic lupus erythematosus. Intra-Articular The intra-articular or soft tissue administration of KENALOG-40 Injection and KENALOG-80 Injection are indicated as adjunctive therapy for short-term administration (to tide the patient over an acute episode or exacerbation) in acute gouty arthritis, acute and subacute bursitis, acute nonspecific tenosynovitis, epicondylitis, rheumatoid arthritis, synovitis of osteoarthritis.
Full extracted label fields
- application numbers
- NDA014901
- boxed warning exact
- brand names
- KENALOG-40
- current indication status
- not_reconciled
- dailymed set url
- https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=d26b97b8-edc8-4b93-b6b9-429016208ff9
- generic names
- TRIAMCINOLONE ACETONIDE
- id
- 008c23fa-2a90-4621-b5a6-cf9262c9319d
- indications and usage exact
- INDICATIONS AND USAGE Intramuscular Where oral therapy is not feasible, injectable corticosteroid therapy, including KENALOG-40 Injection and KENALOG-80 Injection (triamcinolone acetonide injectable suspension, USP) is indicated for intramuscular use 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 and ulcerative colitis. Hematologic disorders: Acquired (autoimmune) hemolytic anemia, Diamond-Blackfan anemia, 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 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, temporal arteritis, 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, polymyositis, and systemic lupus erythematosus. Intra-Articular The intra-articular or soft tissue administration of KENALOG-40 Injection and KENALOG-80 Injection are indicated as adjunctive therapy for short-term administration (to tide the patient over an acute episode or exacerbation) in acute gouty arthritis, acute and subacute bursitis, acute nonspecific tenosynovitis, epicondylitis, rheumatoid arthritis, synovitis of osteoarthritis.
- indications and usage tables exact
- is original packager
- manufacturer names
- A-S Medication Solutions
- matched search terms
- cancer
- lymphomas
- tumor
- package ndcs
- 50090-2360-0
- product ndcs
- 50090-2360
- product types
- HUMAN PRESCRIPTION DRUG
- recent major changes exact
- record type
- complete_spl_indications_section_candidate
- routes
- INTRA-ARTICULAR
- INTRAMUSCULAR
- rxcuis
- 1792144
- 2480108
- 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
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- TRIAMCINOLONE ACETONIDE
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- F446C597KA
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Drugs@FDA application source records
- application number
- NDA014901
- payload
- all indexed label documents
- Appl No
- 014901
- Application Docs Date
- 2006-11-22 00:00:00
- Application Docs ID
- 10850
- Application Docs Title
- 0
- Application Docs Type ID
- 2
- Application Docs URL
- http://www.accessdata.fda.gov/drugsatfda_docs/label/2006/014901s034lbl.pdf
- Submission No
- 34
- Submission Type
- SUPPL
- Appl No
- 014901
- Application Docs Date
- 2010-02-04 00:00:00
- Application Docs ID
- 10851
- Application Docs Title
- 0
- Application Docs Type ID
- 2
- Application Docs URL
- http://www.accessdata.fda.gov/drugsatfda_docs/label/2010/012041s036,014901s037lbl.pdf
- Submission No
- 37
- Submission Type
- SUPPL
- Appl No
- 014901
- Application Docs Date
- 2014-07-09 00:00:00
- Application Docs ID
- 10852
- Application Docs Title
- 0
- Application Docs Type ID
- 2
- Application Docs URL
- http://www.accessdata.fda.gov/drugsatfda_docs/label/2014/014901s042lbledt.pdf
- Submission No
- 42
- Submission Type
- SUPPL
- Appl No
- 014901
- Application Docs Date
- 2011-06-16 00:00:00
- Application Docs ID
- 33127
- Application Docs Title
- 0
- Application Docs Type ID
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- Application Docs URL
- http://www.accessdata.fda.gov/drugsatfda_docs/label/2011/014901s038lbl.pdf
- Submission No
- 38
- Submission Type
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- Appl No
- 014901
- Application Docs Date
- 2011-07-18 00:00:00
- Application Docs ID
- 33128
- Application Docs Title
- 0
- Application Docs Type ID
- 2
- Application Docs URL
- http://www.accessdata.fda.gov/drugsatfda_docs/label/2011/014901s039lbl.pdf
- Submission No
- 39
- Submission Type
- SUPPL
- Appl No
- 014901
- Application Docs Date
- 2018-04-01 00:00:00
- Application Docs ID
- 53573
- Application Docs Title
- 0
- Application Docs Type ID
- 2
- Application Docs URL
- https://www.accessdata.fda.gov/drugsatfda_docs/label/2018/014901s044lbl.pdf
- Submission No
- 44
- Submission Type
- SUPPL
- Appl No
- 014901
- Application Docs Date
- 2018-06-28 00:00:00
- Application Docs ID
- 54712
- Application Docs Title
- 0
- Application Docs Type ID
- 2
- Application Docs URL
- http://www.accessdata.fda.gov/drugsatfda_docs/label/2018/014901s045lbl.pdf
- Submission No
- 45
- Submission Type
- SUPPL
- Appl No
- 014901
- Application Docs Date
- 2020-05-19 00:00:00
- Application Docs ID
- 63087
- Application Docs Title
- 0
- Application Docs Type ID
- 2
- Application Docs URL
- http://www.accessdata.fda.gov/drugsatfda_docs/label/2019/014901Orig1s047lbl.pdf
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- 47
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- 014901
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- 2024-06-06 00:00:00
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- 78680
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- 0
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- http://www.accessdata.fda.gov/drugsatfda_docs/label/2024/014901s054lbl.pdf
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- 54
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- Appl No
- 014901
- Application Docs Date
- 2024-11-18 00:00:00
- Application Docs ID
- 80226
- Application Docs Title
- 0
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- 2
- Application Docs URL
- https://www.accessdata.fda.gov/drugsatfda_docs/label/2024/014901Orig1s055lbl.pdf
- Submission No
- 55
- Submission Type
- SUPPL
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- 014901
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- 4
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- 55
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- AP
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- 2024-08-09 00:00:00
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- 014901
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- Appl No
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- 3
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- 44
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- AP
- Submission Status Date
- 2018-03-29 00:00:00
- Submission Type
- SUPPL
- Submissions Public Notes
- Appl No
- 014901
- Review Priority
- STANDARD
- Submission Class Code ID
- 4
- Submission No
- 43
- Submission Status
- AP
- Submission Status Date
- 2015-10-26 00:00:00
- Submission Type
- SUPPL
- Submissions Public Notes
- Appl No
- 014901
- Review Priority
- STANDARD
- Submission Class Code ID
- 3
- Submission No
- 42
- Submission Status
- AP
- Submission Status Date
- 2014-07-03 00:00:00
- Submission Type
- SUPPL
- Submissions Public Notes
- Appl No
- 014901
- Review Priority
- UNKNOWN
- Submission Class Code ID
- 3
- Submission No
- 39
- Submission Status
- AP
- Submission Status Date
- 2011-07-15 00:00:00
- Submission Type
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- Appl No
- 014901
- Review Priority
- UNKNOWN
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- 2011-06-16 00:00:00
- Submission Type
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- Appl No
- 014901
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- 2010-01-28 00:00:00
- Submission Type
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- Appl No
- 014901
- Review Priority
- STANDARD
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- Appl No
- 014901
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- 2006-11-20 00:00:00
- Submission Type
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- Submissions Public Notes
- application number
- NDA014901
- approval interpretation
- Application linkage and approved submission are not indication-level current approval verification
- current indication status
- not_reconciled
- drugsfda url
- https://www.accessdata.fda.gov/scripts/cder/daf/index.cfm?event=overview.process&ApplNo=014901
- has approved submission record
- true
- latest approved submission date
- 2024-08-09
- 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
- 014901
- Application Docs Date
- 2024-11-18 00:00:00
- Application Docs ID
- 80226
- Application Docs Title
- 0
- Application Docs Type ID
- 2
- Application Docs URL
- https://www.accessdata.fda.gov/drugsatfda_docs/label/2024/014901Orig1s055lbl.pdf
- Submission No
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- official application record
- Appl No
- 014901
- Appl Public Notes
- Appl Type
- NDA
- Sponsor Name
- APOTHECON
- openfda application present
- true
- products
- Active Ingredient
- TRIAMCINOLONE ACETONIDE
- Appl No
- 014901
- Drug Name
- KENALOG-40
- Form
- INJECTABLE;INJECTION
- Product No
- 001
- Reference Drug
- 1
- Reference Standard
- 1
- Strength
- 40MG/ML
- marketing status
- Prescription
- Active Ingredient
- TRIAMCINOLONE ACETONIDE
- Appl No
- 014901
- Drug Name
- KENALOG-80
- Form
- INJECTABLE;INJECTION
- Product No
- 002
- Reference Drug
- 1
- Reference Standard
- 1
- Strength
- 80MG/ML
- marketing status
- Prescription
Source passages and status connections
Passage 1 · indication intro context
- application numbers
- NDA014901
- brand names
- KENALOG-40
- classification reasons
- explicit_positive_indication_predicate
- no_tumor_directed_keyword_in_positive_statement
- incomplete_colon_led_indication_intro
- clinical review status
- pending
- content role
- indication_intro_context
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- exact text
- INDICATIONS AND USAGE Intramuscular Where oral therapy is not feasible, injectable corticosteroid therapy, including KENALOG-40 Injection and KENALOG-80 Injection (triamcinolone acetonide injectable suspension, USP) is indicated for intramuscular use 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
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- 0
- current approval status
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- duplicate text group
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- generic names
- TRIAMCINOLONE ACETONIDE
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- 216
- qualifier mentions
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- source defined aliases
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- exact text
- INDICATIONS AND USAGE Intramuscular Where oral therapy is not feasible, injectable corticosteroid therapy, including KENALOG-40 Injection and KENALOG-80 Injection (triamcinolone acetonide injectable suspension, USP) is indicated for intramuscular use 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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- start
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- source url
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- spl effective date
- 2025-12-05
- spl set id
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- structured fields status
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- Source null
- approval pathway
- Source null
- biomarker and test
- Source null
- disease stage
- Source null
- limitations
- Source null
- line
- Source null
- prior therapy
- Source null
- regimen
- Source null
- tumor histology
- Source null
- use intent
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Passage 2 · unclassified context
- application numbers
- NDA014901
- brand names
- KENALOG-40
- classification reasons
- no_unambiguous_positive_indication_predicate
- clinical review status
- pending
- content role
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- exact text
- 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 a
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- 356
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- generic names
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- source defined aliases
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- exact text
- Dermatologic diseases: Bullous dermatitis herpetiformis, exfoliative erythroderma, mycosis fungoides, pemphigus, severe erythema multiforme (Stevens-Johnson syndrome).
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- source url
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- spl effective date
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- spl set id
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- spl version
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- structured fields status
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- structured indication
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- Source null
- approval pathway
- Source null
- biomarker and test
- Source null
- disease stage
- Source null
- limitations
- Source null
- line
- Source null
- prior therapy
- Source null
- regimen
- Source null
- tumor histology
- Source null
- use intent
- unclear
Passage 3 · unclassified context
- application numbers
- NDA014901
- brand names
- KENALOG-40
- classification reasons
- no_unambiguous_positive_indication_predicate
- clinical review status
- pending
- content role
- unclassified_context
- context span
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- 1307
- end exclusive
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- exact text
- ickness, 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 and ulcerative colitis. Hematologic disorders: Acquired (autoimmune) hemolytic anemia, Diamo
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- current approval status
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- duplicate text group
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- generic names
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- label id
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- positive predicate support span
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Passage 5 · unclassified context
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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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Passage 11 · unclassified context
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Preserved source evidence · Not medical advice
Triangle