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 | 70518-1398-5 | REMEDYREPACK INC. | ANDA207812 | HUMAN PRESCRIPTION DRUG | ANDA |
| METHOTREXATE SODIUM | 71335-1118-6 | Bryant Ranch Prepack | ANDA081235 | HUMAN PRESCRIPTION DRUG | ANDA |
| METHOTREXATE SODIUM | 71335-1772-8 | Bryant Ranch Prepack | ANDA213343 | 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 | 71335-2221-1 | Bryant Ranch Prepack | ANDA210454 | HUMAN PRESCRIPTION DRUG | ANDA |
| METHOTREXATE | 68382-775-77 | Zydus Pharmaceuticals USA Inc. | ANDA207812 | HUMAN PRESCRIPTION DRUG | ANDA |
| METHOTREXATE SODIUM | 51285-366-01 | Teva Women's Health, Inc. | ANDA040385 | HUMAN PRESCRIPTION DRUG | ANDA |
| METHOTREXATE SODIUM | 0555-0572-02 | Teva Pharmaceuticals USA, Inc. | ANDA081099 | HUMAN PRESCRIPTION DRUG | ANDA |
| METHOTREXATE SODIUM | 59651-182-36 | Aurobindo Pharma Limited | ANDA210454 | HUMAN PRESCRIPTION DRUG | ANDA |
| METHOTREXATE SODIUM | 0378-0014-01 | Mylan Pharmaceuticals Inc. | ANDA081235 | HUMAN PRESCRIPTION DRUG | ANDA |
| METHOTREXATE SODIUM | 0703-3671-01 | Teva Parenteral Medicines, Inc. | ANDA040843 | HUMAN PRESCRIPTION DRUG | ANDA |
| METHOTREXATE SODIUM | 69238-1423-1 | Amneal Pharmaceuticals NY LLC | ANDA210040 | HUMAN PRESCRIPTION DRUG | ANDA |
| METHOTREXATE SODIUM | 71335-2221-8 | Bryant Ranch Prepack | ANDA210454 | HUMAN PRESCRIPTION DRUG | ANDA |
| METHOTREXATE SODIUM | 0054-4550-15 | Hikma Pharmaceuticals USA Inc. | ANDA040054 | HUMAN PRESCRIPTION DRUG | ANDA |
| METHOTREXATE | 70771-1058-7 | Zydus Lifesciences Limited | ANDA207812 | HUMAN PRESCRIPTION DRUG | ANDA |
| METHOTREXATE SODIUM | 50090-2345-9 | A-S Medication Solutions | ANDA081099 | HUMAN PRESCRIPTION DRUG | ANDA |
| METHOTREXATE | 70771-1058-1 | Zydus Lifesciences Limited | ANDA207812 | HUMAN PRESCRIPTION DRUG | ANDA |
| METHOTREXATE | 68382-775-01 | Zydus Pharmaceuticals USA Inc. | ANDA207812 | HUMAN PRESCRIPTION DRUG | ANDA |
| METHOTREXATE | 68382-775-10 | Zydus Pharmaceuticals USA Inc. | ANDA207812 | HUMAN PRESCRIPTION DRUG | ANDA |
| METHOTREXATE SODIUM | 71335-1772-2 | Bryant Ranch Prepack | ANDA213343 | HUMAN PRESCRIPTION DRUG | ANDA |
| METHOTREXATE | 0143-9519-10 | Hikma Pharmaceuticals USA Inc. | ANDA089340 | HUMAN PRESCRIPTION DRUG | ANDA |
| METHOTREXATE | 0143-9830-01 | Hikma Pharmaceuticals USA Inc. | ANDA040632 | HUMAN PRESCRIPTION DRUG | ANDA |
| METHOTREXATE SODIUM | 70518-3263-1 | REMEDYREPACK INC. | ANDA213343 | HUMAN PRESCRIPTION DRUG | ANDA |
| METHOTREXATE SODIUM | 0555-0572-35 | Teva Pharmaceuticals USA, Inc. | ANDA081099 | HUMAN PRESCRIPTION DRUG | ANDA |
| METHOTREXATE | 70771-1058-3 | Zydus Lifesciences Limited | ANDA207812 | HUMAN PRESCRIPTION DRUG | ANDA |
| METHOTREXATE SODIUM | 51285-367-01 | Teva Women's Health, Inc. | ANDA040385 | HUMAN PRESCRIPTION DRUG | ANDA |
| METHOTREXATE SODIUM | 71335-2221-7 | Bryant Ranch Prepack | ANDA210454 | HUMAN PRESCRIPTION DRUG | ANDA |
| METHOTREXATE | 70771-1058-2 | Zydus Lifesciences Limited | ANDA207812 | HUMAN PRESCRIPTION DRUG | ANDA |
| METHOTREXATE SODIUM | 0703-3678-81 | Teva Parenteral Medicines, Inc. | ANDA040843 | HUMAN PRESCRIPTION DRUG | ANDA |
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