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 | 0054-4550-15 | Hikma Pharmaceuticals USA Inc. | ANDA040054 | HUMAN PRESCRIPTION DRUG | ANDA |
| METHOTREXATE SODIUM | 0054-4550-25 | Hikma Pharmaceuticals USA Inc. | ANDA040054 | HUMAN PRESCRIPTION DRUG | ANDA |
| METHOTREXATE SODIUM | 0054-8550-25 | Hikma Pharmaceuticals USA Inc. | ANDA040054 | HUMAN PRESCRIPTION DRUG | ANDA |
| METHOTREXATE | 0143-9367-01 | Hikma Pharmaceuticals USA Inc. | ANDA040632 | HUMAN PRESCRIPTION DRUG | ANDA |
| METHOTREXATE | 0143-9516-01 | Hikma Pharmaceuticals USA Inc. | ANDA089343 | HUMAN PRESCRIPTION DRUG | ANDA |
| METHOTREXATE | 0143-9517-01 | Hikma Pharmaceuticals USA Inc. | ANDA089342 | HUMAN PRESCRIPTION DRUG | ANDA |
| METHOTREXATE | 0143-9518-01 | Hikma Pharmaceuticals USA Inc. | ANDA089341 | 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 | 0378-0014-01 | Mylan Pharmaceuticals Inc. | ANDA081235 | HUMAN PRESCRIPTION DRUG | ANDA |
| METHOTREXATE SODIUM | 0555-0572-02 | Teva Pharmaceuticals USA, Inc. | ANDA081099 | HUMAN PRESCRIPTION DRUG | ANDA |
| METHOTREXATE SODIUM | 0555-0572-35 | Teva Pharmaceuticals USA, Inc. | ANDA081099 | HUMAN PRESCRIPTION DRUG | ANDA |
| METHOTREXATE SODIUM | 0703-3671-01 | 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 | 0703-3678-01 | Teva Parenteral Medicines, Inc. | ANDA040843 | HUMAN PRESCRIPTION DRUG | ANDA |
| METHOTREXATE SODIUM | 0703-3678-81 | Teva Parenteral Medicines, Inc. | ANDA040843 | HUMAN PRESCRIPTION DRUG | ANDA |
| METHOTREXATE | 0904-7141-10 | Major Pharmaceuticals | ANDA207812 | HUMAN PRESCRIPTION DRUG | ANDA |
| METHOTREXATE | 16729-277-03 | Accord Healthcare, Inc. | ANDA040716 | HUMAN PRESCRIPTION DRUG | ANDA |
| METHOTREXATE | 16729-277-30 | Accord Healthcare, Inc. | ANDA040716 | HUMAN PRESCRIPTION DRUG | ANDA |
| METHOTREXATE | 16729-277-35 | Accord Healthcare, Inc. | ANDA040716 | HUMAN PRESCRIPTION DRUG | ANDA |
| METHOTREXATE SODIUM | 16729-486-01 | Accord Healthcare Inc. | ANDA213343 | HUMAN PRESCRIPTION DRUG | ANDA |
| METHOTREXATE SODIUM | 16729-486-36 | Accord Healthcare Inc. | ANDA213343 | HUMAN PRESCRIPTION DRUG | ANDA |
| METHOTREXATE SODIUM | 21695-111-00 | Rebel Distributors Corp. | ANDA081099 | HUMAN PRESCRIPTION DRUG | ANDA |
| METHOTREXATE SODIUM | 21695-111-30 | Rebel Distributors Corp. | ANDA081099 | HUMAN PRESCRIPTION DRUG | ANDA |
| METHOTREXATE SODIUM | 42254-110-30 | Rebel Distributors Corp. | NDA008085 | HUMAN PRESCRIPTION DRUG | NDA |
| METHOTREXATE SODIUM | 42291-505-01 | AvKARE | ANDA210040 | HUMAN PRESCRIPTION DRUG | ANDA |
| METHOTREXATE SODIUM | 47335-235-83 | Sun Pharmaceutical Industries, Inc. | ANDA201749 | HUMAN PRESCRIPTION DRUG | ANDA |
| METHOTREXATE SODIUM | 47335-235-96 | Sun Pharmaceutical Industries, Inc. | ANDA201749 | HUMAN PRESCRIPTION DRUG | ANDA |
| METHOTREXATE SODIUM | 50090-2345-4 | A-S Medication Solutions | ANDA081099 | HUMAN PRESCRIPTION DRUG | ANDA |
| METHOTREXATE SODIUM | 50090-2345-9 | A-S Medication Solutions | ANDA081099 | HUMAN PRESCRIPTION DRUG | ANDA |
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