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 | 71335-1772-1 | Bryant Ranch Prepack | ANDA213343 | HUMAN PRESCRIPTION DRUG | ANDA |
| METHOTREXATE SODIUM | 71335-1772-2 | Bryant Ranch Prepack | ANDA213343 | HUMAN PRESCRIPTION DRUG | ANDA |
| METHOTREXATE SODIUM | 71335-1772-3 | Bryant Ranch Prepack | ANDA213343 | HUMAN PRESCRIPTION DRUG | ANDA |
| METHOTREXATE SODIUM | 71335-1772-4 | Bryant Ranch Prepack | ANDA213343 | HUMAN PRESCRIPTION DRUG | ANDA |
| METHOTREXATE SODIUM | 71335-1772-5 | Bryant Ranch Prepack | ANDA213343 | HUMAN PRESCRIPTION DRUG | ANDA |
| METHOTREXATE SODIUM | 71335-1772-6 | Bryant Ranch Prepack | ANDA213343 | HUMAN PRESCRIPTION DRUG | ANDA |
| METHOTREXATE SODIUM | 71335-1772-7 | Bryant Ranch Prepack | ANDA213343 | 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 |
| METHOTREXATE SODIUM | 71335-2221-2 | Bryant Ranch Prepack | ANDA210454 | HUMAN PRESCRIPTION DRUG | ANDA |
| METHOTREXATE SODIUM | 71335-2221-3 | Bryant Ranch Prepack | ANDA210454 | HUMAN PRESCRIPTION DRUG | ANDA |
| METHOTREXATE SODIUM | 71335-2221-4 | Bryant Ranch Prepack | ANDA210454 | HUMAN PRESCRIPTION DRUG | ANDA |
| METHOTREXATE SODIUM | 71335-2221-5 | Bryant Ranch Prepack | ANDA210454 | HUMAN PRESCRIPTION DRUG | ANDA |
| METHOTREXATE SODIUM | 71335-2221-6 | Bryant Ranch Prepack | ANDA210454 | HUMAN PRESCRIPTION DRUG | ANDA |
| METHOTREXATE SODIUM | 71335-2221-7 | Bryant Ranch Prepack | ANDA210454 | HUMAN PRESCRIPTION DRUG | ANDA |
| METHOTREXATE SODIUM | 71335-2221-8 | Bryant Ranch Prepack | ANDA210454 | HUMAN PRESCRIPTION DRUG | ANDA |
| METHOTREXATE SODIUM | 72162-2174-1 | Bryant Ranch Prepack | ANDA201749 | HUMAN PRESCRIPTION DRUG | ANDA |
| METHOTREXATE SODIUM | 75840-111-00 | GenPak Solutions LLC | NDA008085 | HUMAN PRESCRIPTION DRUG | NDA |
| METHOTREXATE SODIUM | 75840-111-01 | GenPak Solutions LLC | NDA008085 | HUMAN PRESCRIPTION DRUG | NDA |
| METHOTREXATE | 81927-204-01 | SHORLA ONCOLOGY INC. | NDA212479 | HUMAN PRESCRIPTION DRUG | NDA |
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