• Decrease font size
  • Return font size to normal
  • Increase font size
U.S. Department of Health and Human Services

FDA Application

  • Print
  • Share
  • E-mail
-

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 69238-1423-1  Amneal Pharmaceuticals NY LLC  ANDA210040  HUMAN PRESCRIPTION DRUG  ANDA 
METHOTREXATE SODIUM 69238-1423-6  Amneal Pharmaceuticals NY LLC  ANDA210040  HUMAN PRESCRIPTION DRUG  ANDA 
METHOTREXATE 70518-1398-0  REMEDYREPACK INC.  ANDA207812  HUMAN PRESCRIPTION DRUG  ANDA 
METHOTREXATE 70518-1398-1  REMEDYREPACK INC.  ANDA207812  HUMAN PRESCRIPTION DRUG  ANDA 
METHOTREXATE 70518-1398-2  REMEDYREPACK INC.  ANDA207812  HUMAN PRESCRIPTION DRUG  ANDA 
METHOTREXATE 70518-1398-3  REMEDYREPACK INC.  ANDA207812  HUMAN PRESCRIPTION DRUG  ANDA 
METHOTREXATE 70518-1398-4  REMEDYREPACK INC.  ANDA207812  HUMAN PRESCRIPTION DRUG  ANDA 
METHOTREXATE 70518-1398-5  REMEDYREPACK INC.  ANDA207812  HUMAN PRESCRIPTION DRUG  ANDA 
METHOTREXATE SODIUM 70518-3263-0  REMEDYREPACK INC.  ANDA213343  HUMAN PRESCRIPTION DRUG  ANDA 
METHOTREXATE SODIUM 70518-3263-1  REMEDYREPACK INC.  ANDA213343  HUMAN PRESCRIPTION DRUG  ANDA 
METHOTREXATE SODIUM 70518-3263-2  REMEDYREPACK INC.  ANDA213343  HUMAN PRESCRIPTION DRUG  ANDA 
METHOTREXATE SODIUM 70518-3263-3  REMEDYREPACK INC.  ANDA213343  HUMAN PRESCRIPTION DRUG  ANDA 
METHOTREXATE SODIUM 70518-3263-4  REMEDYREPACK INC.  ANDA213343  HUMAN PRESCRIPTION DRUG  ANDA 
METHOTREXATE SODIUM 70518-3672-0  REMEDYREPACK INC.  ANDA210454  HUMAN PRESCRIPTION DRUG  ANDA 
METHOTREXATE SODIUM 70518-3777-0  REMEDYREPACK INC.  ANDA081099  HUMAN PRESCRIPTION DRUG  ANDA 
METHOTREXATE 70771-1058-0  Zydus Lifesciences Limited  ANDA207812  HUMAN PRESCRIPTION DRUG  ANDA 
METHOTREXATE 70771-1058-1  Zydus Lifesciences Limited  ANDA207812  HUMAN PRESCRIPTION DRUG  ANDA 
METHOTREXATE 70771-1058-2  Zydus Lifesciences Limited  ANDA207812  HUMAN PRESCRIPTION DRUG  ANDA 
METHOTREXATE 70771-1058-3  Zydus Lifesciences Limited  ANDA207812  HUMAN PRESCRIPTION DRUG  ANDA 
METHOTREXATE 70771-1058-5  Zydus Lifesciences Limited  ANDA207812  HUMAN PRESCRIPTION DRUG  ANDA 
METHOTREXATE 70771-1058-7  Zydus Lifesciences Limited  ANDA207812  HUMAN PRESCRIPTION DRUG  ANDA 
METHOTREXATE 70771-1058-9  Zydus Lifesciences Limited  ANDA207812  HUMAN PRESCRIPTION DRUG  ANDA 
METHOTREXATE SODIUM 71335-1118-1  Bryant Ranch Prepack  ANDA081235  HUMAN PRESCRIPTION DRUG  ANDA 
METHOTREXATE SODIUM 71335-1118-2  Bryant Ranch Prepack  ANDA081235  HUMAN PRESCRIPTION DRUG  ANDA 
METHOTREXATE SODIUM 71335-1118-3  Bryant Ranch Prepack  ANDA081235  HUMAN PRESCRIPTION DRUG  ANDA 
METHOTREXATE SODIUM 71335-1118-4  Bryant Ranch Prepack  ANDA081235  HUMAN PRESCRIPTION DRUG  ANDA 
METHOTREXATE SODIUM 71335-1118-5  Bryant Ranch Prepack  ANDA081235  HUMAN PRESCRIPTION DRUG  ANDA 
METHOTREXATE SODIUM 71335-1118-6  Bryant Ranch Prepack  ANDA081235  HUMAN PRESCRIPTION DRUG  ANDA 
METHOTREXATE SODIUM 71335-1118-7  Bryant Ranch Prepack  ANDA081235  HUMAN PRESCRIPTION DRUG  ANDA 
METHOTREXATE SODIUM 71335-1118-8  Bryant Ranch Prepack  ANDA081235  HUMAN PRESCRIPTION DRUG  ANDA 
1-30 31-60 61-90 91-120 121-150 151-170

Return to the FDA Label Search Page

-
-