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 |
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METHOTREXATE | 54436-025-02 | Antares Pharma, Inc. | NDA204824 | HUMAN PRESCRIPTION DRUG | NDA |
METHOTREXATE SODIUM | 70518-3263-2 | REMEDYREPACK INC. | ANDA213343 | HUMAN PRESCRIPTION DRUG | ANDA |
METHOTREXATE SODIUM | 50090-5457-2 | A-S Medication Solutions | ANDA081099 | HUMAN PRESCRIPTION DRUG | ANDA |
METHOTREXATE | 70771-1058-0 | Zydus Lifesciences Limited | ANDA207812 | HUMAN PRESCRIPTION DRUG | ANDA |
METHOTREXATE | 70518-1398-1 | REMEDYREPACK INC. | ANDA207812 | HUMAN PRESCRIPTION DRUG | ANDA |
METHOTREXATE SODIUM | 63323-123-10 | Fresenius Kabi USA, LLC | ANDA040263 | HUMAN PRESCRIPTION DRUG | ANDA |
METHOTREXATE | 54436-025-04 | Antares Pharma, Inc. | NDA204824 | HUMAN PRESCRIPTION DRUG | NDA |
METHOTREXATE | 52652-2001-6 | Azurity Pharmaceuticals, Inc. | NDA208400 | HUMAN PRESCRIPTION DRUG | NDA |
METHOTREXATE | 54436-015-03 | Antares Pharma, Inc. | NDA204824 | HUMAN PRESCRIPTION DRUG | NDA |
METHOTREXATE | 54436-017-02 | Antares Pharma, Inc. | NDA204824 | HUMAN PRESCRIPTION DRUG | NDA |
METHOTREXATE SODIUM | 71335-1118-3 | Bryant Ranch Prepack | ANDA081235 | HUMAN PRESCRIPTION DRUG | ANDA |
METHOTREXATE SODIUM | 71335-1772-7 | Bryant Ranch Prepack | ANDA213343 | HUMAN PRESCRIPTION DRUG | ANDA |
METHOTREXATE SODIUM | 51285-369-01 | Teva Women's Health, Inc. | ANDA040385 | HUMAN PRESCRIPTION DRUG | ANDA |
METHOTREXATE | 16729-277-03 | Accord Healthcare, Inc. | ANDA040716 | HUMAN PRESCRIPTION DRUG | ANDA |
METHOTREXATE | 70518-1398-2 | REMEDYREPACK INC. | ANDA207812 | HUMAN PRESCRIPTION DRUG | ANDA |
METHOTREXATE | 54436-022-04 | Antares Pharma, Inc. | NDA204824 | HUMAN PRESCRIPTION DRUG | NDA |
METHOTREXATE | 54436-010-04 | Antares Pharma, Inc. | NDA204824 | HUMAN PRESCRIPTION DRUG | NDA |
METHOTREXATE | 54436-022-02 | Antares Pharma, Inc. | NDA204824 | HUMAN PRESCRIPTION DRUG | NDA |
METHOTREXATE | 54436-020-01 | Antares Pharma, Inc. | NDA204824 | HUMAN PRESCRIPTION DRUG | NDA |
METHOTREXATE SODIUM | 71335-1772-5 | Bryant Ranch Prepack | ANDA213343 | HUMAN PRESCRIPTION DRUG | ANDA |
METHOTREXATE SODIUM | 0054-8550-25 | Hikma Pharmaceuticals USA Inc. | ANDA040054 | HUMAN PRESCRIPTION DRUG | ANDA |
METHOTREXATE SODIUM | 71335-2221-2 | Bryant Ranch Prepack | ANDA210454 | HUMAN PRESCRIPTION DRUG | ANDA |
METHOTREXATE SODIUM | 42254-110-30 | Rebel Distributors Corp. | NDA008085 | HUMAN PRESCRIPTION DRUG | NDA |
METHOTREXATE SODIUM | 70518-3263-3 | REMEDYREPACK INC. | ANDA213343 | HUMAN PRESCRIPTION DRUG | ANDA |
METHOTREXATE SODIUM | 51407-121-01 | Golden State Medical Supply, Inc. | ANDA081235 | HUMAN PRESCRIPTION DRUG | ANDA |
METHOTREXATE SODIUM | 61703-124-40 | Hospira, Inc. | NDA011719 | HUMAN PRESCRIPTION DRUG | NDA |
METHOTREXATE SODIUM | 59137-515-00 | Medexus Pharma Inc. | NDA205776 | HUMAN PRESCRIPTION DRUG | NDA |
METHOTREXATE SODIUM | 71335-2221-6 | Bryant Ranch Prepack | ANDA210454 | HUMAN PRESCRIPTION DRUG | ANDA |
METHOTREXATE | 70518-1398-4 | REMEDYREPACK INC. | ANDA207812 | HUMAN PRESCRIPTION DRUG | ANDA |
METHOTREXATE | 70518-1398-3 | REMEDYREPACK INC. | ANDA207812 | HUMAN PRESCRIPTION DRUG | ANDA |
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