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 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 SODIUM | 63323-123-10 | Fresenius Kabi USA, LLC | ANDA040263 | HUMAN PRESCRIPTION DRUG | ANDA |
METHOTREXATE SODIUM | 59137-530-00 | Medexus Pharma Inc. | NDA205776 | HUMAN PRESCRIPTION DRUG | NDA |
METHOTREXATE SODIUM | 0703-3678-01 | Teva Parenteral Medicines, Inc. | ANDA040843 | HUMAN PRESCRIPTION DRUG | ANDA |
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 SODIUM | 21695-111-00 | Rebel Distributors Corp. | ANDA081099 | HUMAN PRESCRIPTION DRUG | ANDA |
METHOTREXATE SODIUM | 61703-408-41 | Hospira, Inc. | NDA011719 | HUMAN PRESCRIPTION DRUG | NDA |
METHOTREXATE SODIUM | 59137-515-04 | Medexus Pharma Inc. | NDA205776 | HUMAN PRESCRIPTION DRUG | NDA |
METHOTREXATE SODIUM | 66336-338-21 | Dispensing Solutions, Inc. | NDA008085 | HUMAN PRESCRIPTION DRUG | NDA |
METHOTREXATE SODIUM | 70518-3263-0 | REMEDYREPACK INC. | ANDA213343 | HUMAN PRESCRIPTION DRUG | ANDA |
METHOTREXATE SODIUM | 51079-670-01 | Mylan Institutional Inc. | ANDA081235 | HUMAN PRESCRIPTION DRUG | ANDA |
METHOTREXATE SODIUM | 16729-486-36 | Accord Healthcare Inc. | ANDA213343 | HUMAN PRESCRIPTION DRUG | ANDA |
METHOTREXATE SODIUM | 70518-3777-0 | REMEDYREPACK INC. | ANDA081099 | HUMAN PRESCRIPTION DRUG | ANDA |
METHOTREXATE SODIUM | 47335-235-96 | Sun Pharmaceutical Industries, Inc. | ANDA201749 | HUMAN PRESCRIPTION DRUG | ANDA |
METHOTREXATE SODIUM | 59137-535-00 | Medexus Pharma Inc. | NDA205776 | HUMAN PRESCRIPTION DRUG | NDA |
METHOTREXATE SODIUM | 71335-2221-5 | Bryant Ranch Prepack | ANDA210454 | HUMAN PRESCRIPTION DRUG | ANDA |
METHOTREXATE SODIUM | 75840-111-00 | GenPak Solutions LLC | NDA008085 | HUMAN PRESCRIPTION DRUG | NDA |
METHOTREXATE SODIUM | 0703-3675-01 | Teva Parenteral Medicines, Inc. | ANDA040843 | HUMAN PRESCRIPTION DRUG | ANDA |
METHOTREXATE SODIUM | 51285-368-01 | Teva Women's Health, Inc. | ANDA040385 | HUMAN PRESCRIPTION DRUG | ANDA |
METHOTREXATE SODIUM | 72162-2174-1 | Bryant Ranch Prepack | ANDA201749 | HUMAN PRESCRIPTION DRUG | ANDA |
METHOTREXATE SODIUM | 70518-3263-4 | REMEDYREPACK INC. | ANDA213343 | HUMAN PRESCRIPTION DRUG | ANDA |
METHOTREXATE SODIUM | 61703-350-09 | Hospira, Inc. | NDA011719 | HUMAN PRESCRIPTION DRUG | NDA |
METHOTREXATE SODIUM | 50268-527-15 | AvPAK | ANDA210040 | HUMAN PRESCRIPTION DRUG | ANDA |
METHOTREXATE SODIUM | 0054-4550-25 | Hikma Pharmaceuticals USA Inc. | ANDA040054 | HUMAN PRESCRIPTION DRUG | ANDA |
METHOTREXATE SODIUM | 71335-1772-4 | Bryant Ranch Prepack | ANDA213343 | HUMAN PRESCRIPTION DRUG | ANDA |
METHOTREXATE SODIUM | 69238-1423-6 | Amneal Pharmaceuticals NY LLC | ANDA210040 | HUMAN PRESCRIPTION DRUG | ANDA |
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