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 | 54436-010-04 | Antares Pharma, Inc. | NDA204824 | HUMAN PRESCRIPTION DRUG | NDA |
| METHOTREXATE | 54436-025-01 | Antares Pharma, Inc. | NDA204824 | HUMAN PRESCRIPTION DRUG | NDA |
| METHOTREXATE | 54436-012-04 | Antares Pharma, Inc. | NDA204824 | HUMAN PRESCRIPTION DRUG | NDA |
| METHOTREXATE | 54436-015-04 | Antares Pharma, Inc. | NDA204824 | HUMAN PRESCRIPTION DRUG | NDA |
| METHOTREXATE | 54436-015-02 | Antares Pharma, Inc. | NDA204824 | HUMAN PRESCRIPTION DRUG | NDA |
| METHOTREXATE SODIUM | 50090-5457-2 | A-S Medication Solutions | ANDA081099 | HUMAN PRESCRIPTION DRUG | ANDA |
| METHOTREXATE SODIUM | 50090-2345-9 | A-S Medication Solutions | ANDA081099 | HUMAN PRESCRIPTION DRUG | ANDA |
| METHOTREXATE SODIUM | 50090-2345-4 | A-S Medication Solutions | ANDA081099 | HUMAN PRESCRIPTION DRUG | ANDA |
| METHOTREXATE SODIUM | 50090-3418-9 | A-S Medication Solutions | ANDA201749 | HUMAN PRESCRIPTION DRUG | ANDA |
| METHOTREXATE SODIUM | 50090-5457-9 | A-S Medication Solutions | ANDA081099 | HUMAN PRESCRIPTION DRUG | ANDA |
| METHOTREXATE SODIUM | 50090-3418-2 | A-S Medication Solutions | ANDA201749 | HUMAN PRESCRIPTION DRUG | ANDA |
| METHOTREXATE SODIUM | 59651-182-36 | Aurobindo Pharma Limited | ANDA210454 | HUMAN PRESCRIPTION DRUG | ANDA |
| METHOTREXATE SODIUM | 59651-182-01 | Aurobindo Pharma Limited | ANDA210454 | HUMAN PRESCRIPTION DRUG | ANDA |
| METHOTREXATE SODIUM | 42291-505-01 | AvKARE | ANDA210040 | HUMAN PRESCRIPTION DRUG | ANDA |
| METHOTREXATE SODIUM | 50268-527-11 | AvPAK | ANDA210040 | HUMAN PRESCRIPTION DRUG | ANDA |
| METHOTREXATE SODIUM | 50268-527-15 | AvPAK | ANDA210040 | HUMAN PRESCRIPTION DRUG | ANDA |
| METHOTREXATE | 52652-2001-1 | Azurity Pharmaceuticals, Inc. | NDA208400 | HUMAN PRESCRIPTION DRUG | NDA |
| METHOTREXATE | 52652-2001-6 | Azurity Pharmaceuticals, Inc. | NDA208400 | HUMAN PRESCRIPTION DRUG | NDA |
| METHOTREXATE SODIUM | 71335-1118-5 | Bryant Ranch Prepack | ANDA081235 | HUMAN PRESCRIPTION DRUG | ANDA |
| METHOTREXATE SODIUM | 71335-1118-7 | Bryant Ranch Prepack | ANDA081235 | HUMAN PRESCRIPTION DRUG | ANDA |
| METHOTREXATE SODIUM | 72162-2174-1 | Bryant Ranch Prepack | ANDA201749 | HUMAN PRESCRIPTION DRUG | ANDA |
| METHOTREXATE SODIUM | 71335-1772-4 | Bryant Ranch Prepack | ANDA213343 | HUMAN PRESCRIPTION DRUG | ANDA |
| METHOTREXATE SODIUM | 71335-2221-5 | Bryant Ranch Prepack | ANDA210454 | HUMAN PRESCRIPTION DRUG | ANDA |
| METHOTREXATE SODIUM | 71335-1118-2 | Bryant Ranch Prepack | ANDA081235 | HUMAN PRESCRIPTION DRUG | ANDA |
| METHOTREXATE SODIUM | 71335-1772-7 | Bryant Ranch Prepack | ANDA213343 | HUMAN PRESCRIPTION DRUG | ANDA |
| METHOTREXATE SODIUM | 71335-2221-2 | Bryant Ranch Prepack | ANDA210454 | HUMAN PRESCRIPTION DRUG | ANDA |
| METHOTREXATE SODIUM | 71335-1772-5 | Bryant Ranch Prepack | ANDA213343 | HUMAN PRESCRIPTION DRUG | ANDA |
| METHOTREXATE SODIUM | 71335-2221-6 | Bryant Ranch Prepack | ANDA210454 | HUMAN PRESCRIPTION DRUG | ANDA |
| METHOTREXATE SODIUM | 71335-1772-8 | Bryant Ranch Prepack | ANDA213343 | HUMAN PRESCRIPTION DRUG | ANDA |
| METHOTREXATE SODIUM | 71335-2221-1 | Bryant Ranch Prepack | ANDA210454 | HUMAN PRESCRIPTION DRUG | ANDA |
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