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LABELS · 02ee9cf4-c6d6-4239-854e-7c5976977456

Simponi

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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
2025-10-29
Captured
2026-09-09T23:37:39.774134+00:00
Current indication reconciliation
Not reconciled
Boxed warning in this label
  1. WARNING: SERIOUS INFECTIONS AND MALIGNANCY WARNING: SERIOUS INFECTIONS AND MALIGNANCY See full prescribing information for complete boxed warning. Serious infections leading to hospitalization or death including tuberculosis (TB), bacterial sepsis, invasive fungal (such as histoplasmosis), and other opportunistic infections have occurred in patients receiving SIMPONI ( 5.1 ) Discontinue SIMPONI if a patient develops a serious infection or sepsis ( 5.1 ) Perform test for latent TB; if positive, start treatment for TB prior to starting SIMPONI ( 5.1 ) Monitor all patients for active TB during treatment, even if initial latent TB test is negative ( 5.1 ) Lymphoma and other malignancies, some fatal, have been reported in children and adolescent patients treated with TNF blockers, of which SIMPONI is a member ( 5.2 ) SERIOUS INFECTIONS Patients treated with SIMPONI are at increased risk for developing serious infections that may lead to hospitalization or death [see Warnings and Precautions (5.1) ] . Most patients who developed these infections were taking concomitant immunosuppressants such as methotrexate or corticosteroids. Discontinue SIMPONI if a patient develops a serious infection. Reported infections with TNF blockers, of which SIMPONI is a member, include: Active tuberculosis, including reactivation of latent tuberculosis. Patients with tuberculosis have frequently presented with disseminated or extrapulmonary disease. Test patients for latent tuberculosis before SIMPONI use and during therapy. Initiate treatment for latent TB prior to SIMPONI use. Invasive fungal infections including histoplasmosis, coccidioidomycosis, candidiasis, aspergillosis, blastomycosis, and pneumocystosis. Patients with histoplasmosis or other invasive fungal infections may present with disseminated, rather than localized, disease. Antigen and antibody testing for histoplasmosis may be negative in some patients with active infection. Consider empiric antifungal therapy in patients at risk for invasive fungal infections who develop severe systemic illness. Bacterial, viral, and other infections due to opportunistic pathogens, including Legionella and Listeria. Consider the risks and benefits of treatment with SIMPONI prior to initiating therapy in patients with chronic or recurrent infection. Monitor patients closely for the development of signs and symptoms of infection during and after treatment with SIMPONI, including the possible development of tuberculosis in patients who tested negative for latent tuberculosis infection prior to initiating therapy [see Warnings and Precautions (5.1) ] . MALIGNANCY Lymphoma and other malignancies, some fatal, have been reported in children and adolescent patients treated with TNF blockers, of which SIMPONI is a member [see Warnings and Precautions (5.2) ] .

Indications and usage: exact source text

  1. 1 INDICATIONS AND USAGE SIMPONI is a tumor necrosis factor (TNF) blocker indicated for the treatment of: adult patients with moderately to severely active rheumatoid arthritis (RA) in combination with methotrexate ( 1.1 ) adult patients with active psoriatic arthritis (PsA) alone, or in combination with methotrexate ( 1.2 ) adult patients with active ankylosing spondylitis (AS) ( 1.3 ) adult and pediatric patients weighing at least 15 kg with moderately to severely active ulcerative colitis (UC) ( 1.4 ) 1.1 Rheumatoid Arthritis SIMPONI, in combination with methotrexate, is indicated for the treatment of adult patients with moderately to severely active rheumatoid arthritis. 1.2 Psoriatic Arthritis SIMPONI, alone or in combination with methotrexate, is indicated for the treatment of adult patients with active psoriatic arthritis. 1.3 Ankylosing Spondylitis SIMPONI is indicated for the treatment of adult patients with active ankylosing spondylitis. 1.4 Ulcerative Colitis SIMPONI is indicated for the treatment of adults and pediatric patients weighing at least 15 kg with moderately to severely active ulcerative colitis .
Full extracted label fields
application numbers
  1. BLA125289
boxed warning exact
  1. WARNING: SERIOUS INFECTIONS AND MALIGNANCY WARNING: SERIOUS INFECTIONS AND MALIGNANCY See full prescribing information for complete boxed warning. Serious infections leading to hospitalization or death including tuberculosis (TB), bacterial sepsis, invasive fungal (such as histoplasmosis), and other opportunistic infections have occurred in patients receiving SIMPONI ( 5.1 ) Discontinue SIMPONI if a patient develops a serious infection or sepsis ( 5.1 ) Perform test for latent TB; if positive, start treatment for TB prior to starting SIMPONI ( 5.1 ) Monitor all patients for active TB during treatment, even if initial latent TB test is negative ( 5.1 ) Lymphoma and other malignancies, some fatal, have been reported in children and adolescent patients treated with TNF blockers, of which SIMPONI is a member ( 5.2 ) SERIOUS INFECTIONS Patients treated with SIMPONI are at increased risk for developing serious infections that may lead to hospitalization or death [see Warnings and Precautions (5.1) ] . Most patients who developed these infections were taking concomitant immunosuppressants such as methotrexate or corticosteroids. Discontinue SIMPONI if a patient develops a serious infection. Reported infections with TNF blockers, of which SIMPONI is a member, include: Active tuberculosis, including reactivation of latent tuberculosis. Patients with tuberculosis have frequently presented with disseminated or extrapulmonary disease. Test patients for latent tuberculosis before SIMPONI use and during therapy. Initiate treatment for latent TB prior to SIMPONI use. Invasive fungal infections including histoplasmosis, coccidioidomycosis, candidiasis, aspergillosis, blastomycosis, and pneumocystosis. Patients with histoplasmosis or other invasive fungal infections may present with disseminated, rather than localized, disease. Antigen and antibody testing for histoplasmosis may be negative in some patients with active infection. Consider empiric antifungal therapy in patients at risk for invasive fungal infections who develop severe systemic illness. Bacterial, viral, and other infections due to opportunistic pathogens, including Legionella and Listeria. Consider the risks and benefits of treatment with SIMPONI prior to initiating therapy in patients with chronic or recurrent infection. Monitor patients closely for the development of signs and symptoms of infection during and after treatment with SIMPONI, including the possible development of tuberculosis in patients who tested negative for latent tuberculosis infection prior to initiating therapy [see Warnings and Precautions (5.1) ] . MALIGNANCY Lymphoma and other malignancies, some fatal, have been reported in children and adolescent patients treated with TNF blockers, of which SIMPONI is a member [see Warnings and Precautions (5.2) ] .
brand names
  1. Simponi
current indication status
not_reconciled
dailymed set url
https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=f86cb4a7-c358-4136-ae57-b32bda9bba00
generic names
  1. GOLIMUMAB
id
02ee9cf4-c6d6-4239-854e-7c5976977456
indications and usage exact
  1. 1 INDICATIONS AND USAGE SIMPONI is a tumor necrosis factor (TNF) blocker indicated for the treatment of: adult patients with moderately to severely active rheumatoid arthritis (RA) in combination with methotrexate ( 1.1 ) adult patients with active psoriatic arthritis (PsA) alone, or in combination with methotrexate ( 1.2 ) adult patients with active ankylosing spondylitis (AS) ( 1.3 ) adult and pediatric patients weighing at least 15 kg with moderately to severely active ulcerative colitis (UC) ( 1.4 ) 1.1 Rheumatoid Arthritis SIMPONI, in combination with methotrexate, is indicated for the treatment of adult patients with moderately to severely active rheumatoid arthritis. 1.2 Psoriatic Arthritis SIMPONI, alone or in combination with methotrexate, is indicated for the treatment of adult patients with active psoriatic arthritis. 1.3 Ankylosing Spondylitis SIMPONI is indicated for the treatment of adult patients with active ankylosing spondylitis. 1.4 Ulcerative Colitis SIMPONI is indicated for the treatment of adults and pediatric patients weighing at least 15 kg with moderately to severely active ulcerative colitis .
indications and usage tables exact
    is original packager
    1. true
    manufacturer names
    1. Janssen Biotech, Inc.
    matched search terms
    1. tumor
    package ndcs
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    2. 57894-070-02
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    8. 57894-071-89
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    2. 57894-071
    product types
    1. HUMAN PRESCRIPTION DRUG
    recent major changes exact
    1. Indications and Usage ( 1.4 ) 10/2025 Dosage and Administration ( 2.1 , 2.3 , 2.4 ) 10/2025 Warnings and Precautions ( 5.11 ) 10/2025
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    source url
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    spl effective date
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    spl effective time
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    substance names
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    Drugs@FDA application source records
    1. application number
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      payload
      all indexed label documents
      1. Appl No
        125289
        Application Docs Date
        2009-12-11 00:00:00
        Application Docs ID
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        Application Docs Title
        0
        Application Docs Type ID
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        Application Docs Date
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        Application Docs ID
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        Application Docs Type ID
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      3. Appl No
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        Application Docs Date
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        Submission No
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        SUPPL
      4. Appl No
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        Application Docs Date
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        Application Docs ID
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        Application Docs Title
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      5. Appl No
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        Application Docs Date
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        Application Docs ID
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      6. Appl No
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        Application Docs Date
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        0
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        Submission No
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      7. Appl No
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        Application Docs Date
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        Application Docs ID
        18852
        Application Docs Title
        0
        Application Docs Type ID
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        Submission No
        127
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      8. Appl No
        125289
        Application Docs Date
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        Application Docs ID
        39897
        Application Docs Title
        0
        Application Docs Type ID
        2
        Submission No
        1
        Submission Type
        ORIG
      9. Appl No
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        Application Docs Date
        2010-08-10 00:00:00
        Application Docs ID
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        Application Docs Title
        0
        Application Docs Type ID
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        Submission No
        25
        Submission Type
        SUPPL
      10. Appl No
        125289
        Application Docs Date
        2012-01-11 00:00:00
        Application Docs ID
        39899
        Application Docs Title
        0
        Application Docs Type ID
        2
        Submission No
        38
        Submission Type
        SUPPL
      11. Appl No
        125289
        Application Docs Date
        2012-03-15 00:00:00
        Application Docs ID
        39900
        Application Docs Title
        0
        Application Docs Type ID
        2
        Submission No
        64
        Submission Type
        SUPPL
      12. Appl No
        125289
        Application Docs Date
        2012-11-28 00:00:00
        Application Docs ID
        39901
        Application Docs Title
        0
        Application Docs Type ID
        2
        Submission No
        70
        Submission Type
        SUPPL
      all submission records
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        Submissions Public Notes
      2. Appl No
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        Review Priority
        STANDARD
        Submission Class Code ID
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        Submission No
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        Submissions Public Notes
      3. Appl No
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        Review Priority
        STANDARD
        Submission Class Code ID
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        Submission No
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        Submission Status Date
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      4. Appl No
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        Review Priority
        STANDARD
        Submission Class Code ID
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        Submission Status
        AP
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        Submissions Public Notes
      5. Appl No
        125289
        Review Priority
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      6. Appl No
        125289
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        STANDARD
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        Submissions Public Notes
      7. Appl No
        125289
        Review Priority
        STANDARD
        Submission Class Code ID
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        Submission No
        146
        Submission Status
        AP
        Submission Status Date
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        Submissions Public Notes
      8. Appl No
        125289
        Review Priority
        STANDARD
        Submission Class Code ID
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        Submission No
        141
        Submission Status
        AP
        Submission Status Date
        2018-02-09 00:00:00
        Submission Type
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        Submissions Public Notes
      9. Appl No
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        Review Priority
        STANDARD
        Submission Class Code ID
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        Submission No
        139
        Submission Status
        AP
        Submission Status Date
        2018-03-06 00:00:00
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        Submissions Public Notes
      10. Appl No
        125289
        Review Priority
        STANDARD
        Submission Class Code ID
        3
        Submission No
        137
        Submission Status
        AP
        Submission Status Date
        2017-11-13 00:00:00
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        Submissions Public Notes
      11. Appl No
        125289
        Review Priority
        STANDARD
        Submission Class Code ID
        3
        Submission No
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        Submission Status
        AP
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        Submissions Public Notes
      12. Appl No
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        Review Priority
        STANDARD
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        Submission No
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        Submission Status Date
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        Submissions Public Notes
      application number
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      approval interpretation
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      current indication status
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      latest approved submission date
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      latest label selection rule
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      latest posted label documents
      1. Appl No
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        Application Docs Date
        2025-10-23 00:00:00
        Application Docs ID
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        Application Docs Title
        0
        Application Docs Type ID
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        Submission No
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        Submission Type
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      official application record
      Appl No
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      Appl Public Notes
      Appl Type
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      Sponsor Name
      CENTOCOR ORTHO BIOTECH INC
      openfda application present
      true
      products
      1. Active Ingredient
        GOLIMUMAB
        Appl No
        125289
        Drug Name
        SIMPONI
        Form
        INJECTABLE; INJECTION
        Product No
        001
        Reference Drug
        2
        Reference Standard
        Strength
        50MG
        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
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    brand names
    1. Simponi
    classification reasons
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    1 INDICATIONS AND USAGE SIMPONI is a tumor necrosis factor (TNF) blocker indicated for the treatment of: adult patients with moderately to severely active rheumatoid arthritis (RA) in combination with methotrexate ( 1.1 ) adult patients with active psoriatic arthritis (PsA) alone, or in combination with methotrexate ( 1.2 ) adult patients with active ankylosing spondylitis (AS) ( 1.3 ) adult and pediatric patients wei
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        1 INDICATIONS AND USAGE SIMPONI is a tumor necrosis factor (TNF) blocker indicated for the treatment of: adult patients with moderately to severely active rheumatoid arthritis (RA) in combination with methotrexate ( 1.1 )
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        Passage 2 · positive indication candidate
        application numbers
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        E SIMPONI is a tumor necrosis factor (TNF) blocker indicated for the treatment of: adult patients with moderately to severely active rheumatoid arthritis (RA) in combination with methotrexate ( 1.1 ) adult patients with active psoriatic arthritis (PsA) alone, or in combination with methotrexate ( 1.2 ) adult patients with active ankylosing spondylitis (AS) ( 1.3 ) adult and pediatric patients weighing at least 15 kg with moderately to severely active ulcerative colitis (UC) ( 1.4 ) 1.1 Rheumatoid A
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                            to severely active rheumatoid arthritis. 1.2 Psoriatic Arthritis SIMPONI, alone or in combination with methotrexate, is indicated for the treatment of adult patients with active psoriatic arthritis. 1.3 Ankylosing Spondylitis SIMPONI is indicated for the treatment of adult patients with active ankylosing spondylitis. 1.4 Ulcerative Colitis SIMPONI is indicated for the treatment of adults and pediatric patients weighing at least 15 kg with moderately to severely active ulcerative colitis .
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                                1.3 Ankylosing Spondylitis SIMPONI is indicated for the treatment of adult patients with active ankylosing spondylitis.
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                                indicated for the treatment of adult patients with active psoriatic arthritis. 1.3 Ankylosing Spondylitis SIMPONI is indicated for the treatment of adult patients with active ankylosing spondylitis. 1.4 Ulcerative Colitis SIMPONI is indicated for the treatment of adults and pediatric patients weighing at least 15 kg with moderately to severely active ulcerative colitis .
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                                    1.4 Ulcerative Colitis SIMPONI is indicated for the treatment of adults and pediatric patients weighing at least 15 kg with moderately to severely active ulcerative colitis .
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                                    Preserved source evidence · Not medical advice