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 | 71335-1118-8 | Bryant Ranch Prepack | ANDA081235 | HUMAN PRESCRIPTION DRUG | ANDA |
| METHOTREXATE SODIUM | 71335-1118-1 | Bryant Ranch Prepack | ANDA081235 | HUMAN PRESCRIPTION DRUG | ANDA |
| METHOTREXATE SODIUM | 71335-1118-4 | Bryant Ranch Prepack | ANDA081235 | HUMAN PRESCRIPTION DRUG | ANDA |
| METHOTREXATE SODIUM | 0378-0014-01 | Mylan Pharmaceuticals Inc. | ANDA081235 | HUMAN PRESCRIPTION DRUG | ANDA |
| METHOTREXATE SODIUM | 51079-670-01 | Mylan Institutional Inc. | ANDA081235 | HUMAN PRESCRIPTION DRUG | ANDA |
| METHOTREXATE SODIUM | 71335-1118-3 | Bryant Ranch Prepack | ANDA081235 | HUMAN PRESCRIPTION DRUG | ANDA |
| METHOTREXATE SODIUM | 51079-670-05 | Mylan Institutional Inc. | ANDA081235 | HUMAN PRESCRIPTION DRUG | ANDA |
| METHOTREXATE SODIUM | 71335-1118-2 | Bryant Ranch Prepack | ANDA081235 | HUMAN PRESCRIPTION DRUG | ANDA |
| METHOTREXATE SODIUM | 71335-1118-7 | Bryant Ranch Prepack | ANDA081235 | HUMAN PRESCRIPTION DRUG | ANDA |
| METHOTREXATE | 0143-9519-10 | Hikma Pharmaceuticals USA Inc. | ANDA089340 | HUMAN PRESCRIPTION DRUG | ANDA |
| METHOTREXATE | 0143-9518-01 | Hikma Pharmaceuticals USA Inc. | ANDA089341 | HUMAN PRESCRIPTION DRUG | ANDA |
| METHOTREXATE | 0143-9517-01 | Hikma Pharmaceuticals USA Inc. | ANDA089342 | HUMAN PRESCRIPTION DRUG | ANDA |
| METHOTREXATE | 0143-9516-01 | Hikma Pharmaceuticals USA Inc. | ANDA089343 | HUMAN PRESCRIPTION DRUG | ANDA |
| METHOTREXATE SODIUM | 47335-235-96 | Sun Pharmaceutical Industries, Inc. | ANDA201749 | HUMAN PRESCRIPTION DRUG | ANDA |
| METHOTREXATE SODIUM | 72162-2174-1 | Bryant Ranch Prepack | ANDA201749 | HUMAN PRESCRIPTION DRUG | ANDA |
| METHOTREXATE SODIUM | 50090-3418-2 | A-S Medication Solutions | ANDA201749 | HUMAN PRESCRIPTION DRUG | ANDA |
| METHOTREXATE SODIUM | 47335-235-83 | Sun Pharmaceutical Industries, Inc. | ANDA201749 | HUMAN PRESCRIPTION DRUG | ANDA |
| METHOTREXATE SODIUM | 50090-3418-9 | A-S Medication Solutions | ANDA201749 | HUMAN PRESCRIPTION DRUG | ANDA |
| METHOTREXATE | 70771-1058-3 | Zydus Lifesciences Limited | ANDA207812 | HUMAN PRESCRIPTION DRUG | ANDA |
| METHOTREXATE | 70518-1398-0 | REMEDYREPACK INC. | ANDA207812 | HUMAN PRESCRIPTION DRUG | ANDA |
| METHOTREXATE | 70771-1058-5 | Zydus Lifesciences Limited | ANDA207812 | HUMAN PRESCRIPTION DRUG | ANDA |
| METHOTREXATE | 68382-775-05 | Zydus Pharmaceuticals USA Inc. | ANDA207812 | HUMAN PRESCRIPTION DRUG | ANDA |
| METHOTREXATE | 70771-1058-0 | Zydus Lifesciences Limited | ANDA207812 | HUMAN PRESCRIPTION DRUG | ANDA |
| METHOTREXATE | 70518-1398-1 | REMEDYREPACK INC. | ANDA207812 | HUMAN PRESCRIPTION DRUG | ANDA |
| METHOTREXATE | 0904-7141-10 | Major Pharmaceuticals | ANDA207812 | HUMAN PRESCRIPTION DRUG | ANDA |
| METHOTREXATE | 70771-1058-9 | Zydus Lifesciences Limited | ANDA207812 | HUMAN PRESCRIPTION DRUG | ANDA |
| METHOTREXATE | 70518-1398-5 | REMEDYREPACK INC. | ANDA207812 | HUMAN PRESCRIPTION DRUG | ANDA |
| METHOTREXATE | 68382-775-60 | Zydus Pharmaceuticals USA Inc. | ANDA207812 | HUMAN PRESCRIPTION DRUG | ANDA |
| METHOTREXATE | 68382-775-16 | Zydus Pharmaceuticals USA Inc. | ANDA207812 | HUMAN PRESCRIPTION DRUG | ANDA |
| METHOTREXATE | 70518-1398-4 | REMEDYREPACK INC. | ANDA207812 | HUMAN PRESCRIPTION DRUG | ANDA |
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