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 | 59137-535-01 | Medexus Pharma Inc. | NDA205776 | HUMAN PRESCRIPTION DRUG | NDA |
| METHOTREXATE SODIUM | 59137-530-04 | Medexus Pharma Inc. | NDA205776 | HUMAN PRESCRIPTION DRUG | NDA |
| METHOTREXATE SODIUM | 59137-525-01 | Medexus Pharma Inc. | NDA205776 | HUMAN PRESCRIPTION DRUG | NDA |
| METHOTREXATE SODIUM | 59137-520-04 | Medexus Pharma Inc. | NDA205776 | HUMAN PRESCRIPTION DRUG | NDA |
| METHOTREXATE SODIUM | 59137-550-01 | Medexus Pharma Inc. | NDA205776 | HUMAN PRESCRIPTION DRUG | NDA |
| METHOTREXATE SODIUM | 51079-670-05 | Mylan Institutional Inc. | ANDA081235 | HUMAN PRESCRIPTION DRUG | ANDA |
| METHOTREXATE SODIUM | 51079-670-01 | Mylan Institutional Inc. | ANDA081235 | HUMAN PRESCRIPTION DRUG | ANDA |
| METHOTREXATE SODIUM | 0378-0014-01 | Mylan Pharmaceuticals Inc. | ANDA081235 | HUMAN PRESCRIPTION DRUG | ANDA |
| METHOTREXATE SODIUM | 21695-111-00 | Rebel Distributors Corp. | ANDA081099 | HUMAN PRESCRIPTION DRUG | ANDA |
| METHOTREXATE SODIUM | 42254-110-30 | Rebel Distributors Corp. | NDA008085 | HUMAN PRESCRIPTION DRUG | NDA |
| METHOTREXATE SODIUM | 21695-111-30 | Rebel Distributors Corp. | ANDA081099 | HUMAN PRESCRIPTION DRUG | ANDA |
| METHOTREXATE | 70518-1398-3 | REMEDYREPACK INC. | ANDA207812 | HUMAN PRESCRIPTION DRUG | ANDA |
| METHOTREXATE | 70518-1398-5 | REMEDYREPACK INC. | ANDA207812 | HUMAN PRESCRIPTION DRUG | ANDA |
| METHOTREXATE | 70518-1398-2 | REMEDYREPACK INC. | ANDA207812 | HUMAN PRESCRIPTION DRUG | ANDA |
| METHOTREXATE SODIUM | 70518-3263-3 | REMEDYREPACK INC. | ANDA213343 | HUMAN PRESCRIPTION DRUG | ANDA |
| METHOTREXATE | 70518-1398-4 | REMEDYREPACK INC. | ANDA207812 | HUMAN PRESCRIPTION DRUG | ANDA |
| METHOTREXATE SODIUM | 70518-3263-2 | REMEDYREPACK INC. | ANDA213343 | HUMAN PRESCRIPTION DRUG | ANDA |
| METHOTREXATE | 70518-1398-1 | REMEDYREPACK INC. | ANDA207812 | HUMAN PRESCRIPTION DRUG | ANDA |
| METHOTREXATE SODIUM | 70518-3263-0 | REMEDYREPACK INC. | ANDA213343 | HUMAN PRESCRIPTION DRUG | ANDA |
| METHOTREXATE SODIUM | 70518-3263-4 | REMEDYREPACK INC. | ANDA213343 | HUMAN PRESCRIPTION DRUG | ANDA |
| METHOTREXATE SODIUM | 70518-3777-0 | REMEDYREPACK INC. | ANDA081099 | HUMAN PRESCRIPTION DRUG | ANDA |
| METHOTREXATE SODIUM | 70518-3672-0 | REMEDYREPACK INC. | ANDA210454 | HUMAN PRESCRIPTION DRUG | ANDA |
| METHOTREXATE SODIUM | 70518-3263-1 | REMEDYREPACK INC. | ANDA213343 | HUMAN PRESCRIPTION DRUG | ANDA |
| METHOTREXATE | 70518-1398-0 | REMEDYREPACK INC. | ANDA207812 | HUMAN PRESCRIPTION DRUG | ANDA |
| METHOTREXATE | 81927-204-01 | SHORLA ONCOLOGY INC. | NDA212479 | HUMAN PRESCRIPTION DRUG | NDA |
| METHOTREXATE SODIUM | 47335-235-96 | Sun Pharmaceutical Industries, Inc. | ANDA201749 | HUMAN PRESCRIPTION DRUG | ANDA |
| METHOTREXATE SODIUM | 47335-235-83 | Sun Pharmaceutical Industries, Inc. | ANDA201749 | HUMAN PRESCRIPTION DRUG | ANDA |
| METHOTREXATE SODIUM | 0703-3678-01 | Teva Parenteral Medicines, Inc. | ANDA040843 | HUMAN PRESCRIPTION DRUG | ANDA |
| METHOTREXATE SODIUM | 0703-3675-01 | Teva Parenteral Medicines, Inc. | ANDA040843 | HUMAN PRESCRIPTION DRUG | ANDA |
| METHOTREXATE SODIUM | 0703-3671-01 | Teva Parenteral Medicines, Inc. | ANDA040843 | HUMAN PRESCRIPTION DRUG | ANDA |
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