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U.S. Department of Health and Human Services

FDA Application
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NDC Search Results on Active Ingredient: methotrexate

Click on Active Ingredient to view the label.

Ingredient Name NDC Company Name Application Number or Regulatory Citation Product Type Marketing Category
METHOTREXATE SODIUM 50090-3418-2  A-S Medication Solutions  ANDA201749  HUMAN PRESCRIPTION DRUG  ANDA 
METHOTREXATE SODIUM 50090-3418-9  A-S Medication Solutions  ANDA201749  HUMAN PRESCRIPTION DRUG  ANDA 
METHOTREXATE SODIUM 50090-5457-2  A-S Medication Solutions  ANDA081099  HUMAN PRESCRIPTION DRUG  ANDA 
METHOTREXATE SODIUM 50090-5457-9  A-S Medication Solutions  ANDA081099  HUMAN PRESCRIPTION DRUG  ANDA 
METHOTREXATE SODIUM 50268-527-11  AvPAK  ANDA210040  HUMAN PRESCRIPTION DRUG  ANDA 
METHOTREXATE SODIUM 50268-527-15  AvPAK  ANDA210040  HUMAN PRESCRIPTION DRUG  ANDA 
METHOTREXATE SODIUM 51079-670-01  Mylan Institutional Inc.  ANDA081235  HUMAN PRESCRIPTION DRUG  ANDA 
METHOTREXATE SODIUM 51079-670-05  Mylan Institutional Inc.  ANDA081235  HUMAN PRESCRIPTION DRUG  ANDA 
METHOTREXATE SODIUM 51285-366-01  Teva Women's Health, Inc.  ANDA040385  HUMAN PRESCRIPTION DRUG  ANDA 
METHOTREXATE SODIUM 51285-367-01  Teva Women's Health, Inc.  ANDA040385  HUMAN PRESCRIPTION DRUG  ANDA 
METHOTREXATE SODIUM 51285-368-01  Teva Women's Health, Inc.  ANDA040385  HUMAN PRESCRIPTION DRUG  ANDA 
METHOTREXATE SODIUM 51285-369-01  Teva Women's Health, Inc.  ANDA040385  HUMAN PRESCRIPTION DRUG  ANDA 
METHOTREXATE SODIUM 51407-121-01  Golden State Medical Supply, Inc.  ANDA081235  HUMAN PRESCRIPTION DRUG  ANDA 
METHOTREXATE 52652-2001-1  Azurity Pharmaceuticals, Inc.  NDA208400  HUMAN PRESCRIPTION DRUG  NDA 
METHOTREXATE 52652-2001-6  Azurity Pharmaceuticals, Inc.  NDA208400  HUMAN PRESCRIPTION DRUG  NDA 
METHOTREXATE 54436-010-01  Antares Pharma, Inc.  NDA204824  HUMAN PRESCRIPTION DRUG  NDA 
METHOTREXATE 54436-010-02  Antares Pharma, Inc.  NDA204824  HUMAN PRESCRIPTION DRUG  NDA 
METHOTREXATE 54436-010-03  Antares Pharma, Inc.  NDA204824  HUMAN PRESCRIPTION DRUG  NDA 
METHOTREXATE 54436-010-04  Antares Pharma, Inc.  NDA204824  HUMAN PRESCRIPTION DRUG  NDA 
METHOTREXATE 54436-012-01  Antares Pharma, Inc.  NDA204824  HUMAN PRESCRIPTION DRUG  NDA 
METHOTREXATE 54436-012-02  Antares Pharma, Inc.  NDA204824  HUMAN PRESCRIPTION DRUG  NDA 
METHOTREXATE 54436-012-03  Antares Pharma, Inc.  NDA204824  HUMAN PRESCRIPTION DRUG  NDA 
METHOTREXATE 54436-012-04  Antares Pharma, Inc.  NDA204824  HUMAN PRESCRIPTION DRUG  NDA 
METHOTREXATE 54436-015-01  Antares Pharma, Inc.  NDA204824  HUMAN PRESCRIPTION DRUG  NDA 
METHOTREXATE 54436-015-02  Antares Pharma, Inc.  NDA204824  HUMAN PRESCRIPTION DRUG  NDA 
METHOTREXATE 54436-015-03  Antares Pharma, Inc.  NDA204824  HUMAN PRESCRIPTION DRUG  NDA 
METHOTREXATE 54436-015-04  Antares Pharma, Inc.  NDA204824  HUMAN PRESCRIPTION DRUG  NDA 
METHOTREXATE 54436-017-01  Antares Pharma, Inc.  NDA204824  HUMAN PRESCRIPTION DRUG  NDA 
METHOTREXATE 54436-017-02  Antares Pharma, Inc.  NDA204824  HUMAN PRESCRIPTION DRUG  NDA 
METHOTREXATE 54436-017-03  Antares Pharma, Inc.  NDA204824  HUMAN PRESCRIPTION DRUG  NDA 
1-30 31-60 61-90 91-120 121-150 151-170

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