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 |
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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 |
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