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 | 59137-535-04 | Medexus Pharma Inc. | NDA205776 | HUMAN PRESCRIPTION DRUG | NDA |
| METHOTREXATE | 54436-020-02 | Antares Pharma, Inc. | NDA204824 | HUMAN PRESCRIPTION DRUG | NDA |
| METHOTREXATE SODIUM | 0378-0014-01 | Mylan Pharmaceuticals Inc. | ANDA081235 | HUMAN PRESCRIPTION DRUG | ANDA |
| METHOTREXATE SODIUM | 61703-350-37 | Hospira, Inc. | NDA011719 | HUMAN PRESCRIPTION DRUG | NDA |
| METHOTREXATE | 54436-022-03 | Antares Pharma, Inc. | NDA204824 | HUMAN PRESCRIPTION DRUG | NDA |
| METHOTREXATE | 54436-017-01 | Antares Pharma, Inc. | NDA204824 | HUMAN PRESCRIPTION DRUG | NDA |
| METHOTREXATE SODIUM | 59137-525-04 | Medexus Pharma Inc. | NDA205776 | HUMAN PRESCRIPTION DRUG | NDA |
| METHOTREXATE SODIUM | 59137-525-00 | Medexus Pharma Inc. | NDA205776 | HUMAN PRESCRIPTION DRUG | NDA |
| METHOTREXATE SODIUM | 59137-550-01 | Medexus Pharma Inc. | NDA205776 | HUMAN PRESCRIPTION DRUG | NDA |
| METHOTREXATE | 0143-9519-10 | Hikma Pharmaceuticals USA Inc. | ANDA089340 | HUMAN PRESCRIPTION DRUG | ANDA |
| METHOTREXATE SODIUM | 0703-3678-81 | Teva Parenteral Medicines, Inc. | ANDA040843 | HUMAN PRESCRIPTION DRUG | ANDA |
| METHOTREXATE SODIUM | 0054-4550-15 | Hikma Pharmaceuticals USA Inc. | ANDA040054 | HUMAN PRESCRIPTION DRUG | ANDA |
| METHOTREXATE SODIUM | 0555-0572-35 | Teva Pharmaceuticals USA, Inc. | ANDA081099 | HUMAN PRESCRIPTION DRUG | ANDA |
| METHOTREXATE SODIUM | 69238-1423-1 | Amneal Pharmaceuticals NY LLC | ANDA210040 | HUMAN PRESCRIPTION DRUG | ANDA |
| METHOTREXATE SODIUM | 50090-2345-9 | A-S Medication Solutions | ANDA081099 | HUMAN PRESCRIPTION DRUG | ANDA |
| METHOTREXATE | 70771-1058-7 | Zydus Lifesciences Limited | ANDA207812 | HUMAN PRESCRIPTION DRUG | ANDA |
| METHOTREXATE SODIUM | 71335-2221-7 | Bryant Ranch Prepack | ANDA210454 | HUMAN PRESCRIPTION DRUG | ANDA |
| METHOTREXATE SODIUM | 61703-408-25 | Hospira, Inc. | NDA011719 | HUMAN PRESCRIPTION DRUG | NDA |
| METHOTREXATE | 0143-9830-01 | Hikma Pharmaceuticals USA Inc. | ANDA040632 | HUMAN PRESCRIPTION DRUG | ANDA |
| METHOTREXATE SODIUM | 51285-367-01 | Teva Women's Health, Inc. | ANDA040385 | HUMAN PRESCRIPTION DRUG | ANDA |
| METHOTREXATE | 70771-1058-3 | Zydus Lifesciences Limited | ANDA207812 | HUMAN PRESCRIPTION DRUG | ANDA |
| METHOTREXATE SODIUM | 70518-3263-1 | REMEDYREPACK INC. | ANDA213343 | HUMAN PRESCRIPTION DRUG | ANDA |
| METHOTREXATE | 54436-012-01 | Antares Pharma, Inc. | NDA204824 | HUMAN PRESCRIPTION DRUG | NDA |
| METHOTREXATE | 54436-017-03 | Antares Pharma, Inc. | NDA204824 | HUMAN PRESCRIPTION DRUG | NDA |
| METHOTREXATE SODIUM | 71335-2221-8 | Bryant Ranch Prepack | ANDA210454 | HUMAN PRESCRIPTION DRUG | ANDA |
| METHOTREXATE SODIUM | 71335-1772-2 | Bryant Ranch Prepack | ANDA213343 | HUMAN PRESCRIPTION DRUG | ANDA |
| METHOTREXATE | 68382-775-01 | Zydus Pharmaceuticals USA Inc. | ANDA207812 | HUMAN PRESCRIPTION DRUG | ANDA |
| METHOTREXATE | 70771-1058-2 | Zydus Lifesciences Limited | ANDA207812 | HUMAN PRESCRIPTION DRUG | ANDA |
| METHOTREXATE | 70771-1058-1 | Zydus Lifesciences Limited | ANDA207812 | HUMAN PRESCRIPTION DRUG | ANDA |
| METHOTREXATE | 68382-775-10 | Zydus Pharmaceuticals USA Inc. | ANDA207812 | HUMAN PRESCRIPTION DRUG | ANDA |
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