FDA Application
-
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 | 71335-1772-6 | Bryant Ranch Prepack | ANDA213343 | HUMAN PRESCRIPTION DRUG | ANDA |
| METHOTREXATE SODIUM | 71335-1118-8 | Bryant Ranch Prepack | ANDA081235 | HUMAN PRESCRIPTION DRUG | ANDA |
| METHOTREXATE SODIUM | 71335-1118-4 | Bryant Ranch Prepack | ANDA081235 | HUMAN PRESCRIPTION DRUG | ANDA |
| METHOTREXATE SODIUM | 71335-2221-1 | Bryant Ranch Prepack | ANDA210454 | HUMAN PRESCRIPTION DRUG | ANDA |
| METHOTREXATE SODIUM | 71335-2221-7 | Bryant Ranch Prepack | ANDA210454 | HUMAN PRESCRIPTION DRUG | ANDA |
| METHOTREXATE SODIUM | 71335-1772-2 | Bryant Ranch Prepack | ANDA213343 | HUMAN PRESCRIPTION DRUG | ANDA |
| METHOTREXATE SODIUM | 71335-1118-6 | Bryant Ranch Prepack | ANDA081235 | HUMAN PRESCRIPTION DRUG | ANDA |
| METHOTREXATE SODIUM | 71335-2221-8 | Bryant Ranch Prepack | ANDA210454 | HUMAN PRESCRIPTION DRUG | ANDA |
| METHOTREXATE SODIUM | 71335-1772-8 | Bryant Ranch Prepack | ANDA213343 | HUMAN PRESCRIPTION DRUG | ANDA |
| METHOTREXATE SODIUM | 71335-2221-2 | Bryant Ranch Prepack | ANDA210454 | HUMAN PRESCRIPTION DRUG | ANDA |
| METHOTREXATE SODIUM | 71335-2221-6 | Bryant Ranch Prepack | ANDA210454 | HUMAN PRESCRIPTION DRUG | ANDA |
| METHOTREXATE SODIUM | 71335-1772-7 | Bryant Ranch Prepack | ANDA213343 | HUMAN PRESCRIPTION DRUG | ANDA |
| METHOTREXATE SODIUM | 71335-1772-5 | Bryant Ranch Prepack | ANDA213343 | HUMAN PRESCRIPTION DRUG | ANDA |
| METHOTREXATE SODIUM | 62135-772-35 | Chartwell RX, LLC | ANDA210454 | HUMAN PRESCRIPTION DRUG | ANDA |
| METHOTREXATE SODIUM | 66336-338-30 | Dispensing Solutions, Inc. | NDA008085 | HUMAN PRESCRIPTION DRUG | NDA |
| METHOTREXATE SODIUM | 66336-338-21 | Dispensing Solutions, Inc. | NDA008085 | HUMAN PRESCRIPTION DRUG | NDA |
| METHOTREXATE SODIUM | 63323-123-10 | Fresenius Kabi USA, LLC | ANDA040263 | HUMAN PRESCRIPTION DRUG | ANDA |
| METHOTREXATE SODIUM | 63323-122-50 | Fresenius Kabi USA, LLC | ANDA040266 | HUMAN PRESCRIPTION DRUG | ANDA |
| METHOTREXATE SODIUM | 75840-111-01 | GenPak Solutions LLC | NDA008085 | HUMAN PRESCRIPTION DRUG | NDA |
| METHOTREXATE SODIUM | 75840-111-00 | GenPak Solutions LLC | NDA008085 | HUMAN PRESCRIPTION DRUG | NDA |
| METHOTREXATE SODIUM | 51407-121-01 | Golden State Medical Supply, Inc. | ANDA081235 | HUMAN PRESCRIPTION DRUG | ANDA |
| METHOTREXATE SODIUM | 0054-8550-25 | Hikma Pharmaceuticals USA Inc. | ANDA040054 | HUMAN PRESCRIPTION DRUG | ANDA |
| METHOTREXATE | 0143-9517-01 | Hikma Pharmaceuticals USA Inc. | ANDA089342 | 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 | 0054-4550-25 | Hikma Pharmaceuticals USA Inc. | ANDA040054 | HUMAN PRESCRIPTION DRUG | ANDA |
| METHOTREXATE | 0143-9516-01 | Hikma Pharmaceuticals USA Inc. | ANDA089343 | HUMAN PRESCRIPTION DRUG | ANDA |
| METHOTREXATE | 0143-9367-01 | Hikma Pharmaceuticals USA Inc. | ANDA040632 | HUMAN PRESCRIPTION DRUG | ANDA |
| METHOTREXATE SODIUM | 0054-4550-15 | Hikma Pharmaceuticals USA Inc. | ANDA040054 | HUMAN PRESCRIPTION DRUG | ANDA |
| METHOTREXATE | 0143-9518-01 | Hikma Pharmaceuticals USA Inc. | ANDA089341 | HUMAN PRESCRIPTION DRUG | ANDA |
| 1-30 | 31-60 | 61-90 | 91-120 | 121-150 | 151-170 |
-
