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 | 59137-525-00 | Medexus Pharma Inc. | NDA205776 | HUMAN PRESCRIPTION DRUG | NDA |
METHOTREXATE SODIUM | 59137-550-01 | Medexus Pharma Inc. | NDA205776 | HUMAN PRESCRIPTION DRUG | NDA |
METHOTREXATE SODIUM | 0703-3671-01 | Teva Parenteral Medicines, Inc. | ANDA040843 | HUMAN PRESCRIPTION DRUG | ANDA |
METHOTREXATE SODIUM | 59137-535-04 | Medexus Pharma Inc. | NDA205776 | HUMAN PRESCRIPTION DRUG | NDA |
METHOTREXATE SODIUM | 71335-1772-8 | Bryant Ranch Prepack | ANDA213343 | HUMAN PRESCRIPTION DRUG | ANDA |
METHOTREXATE SODIUM | 50090-2345-4 | A-S Medication Solutions | ANDA081099 | HUMAN PRESCRIPTION DRUG | ANDA |
METHOTREXATE SODIUM | 59137-510-00 | Medexus Pharma Inc. | NDA205776 | HUMAN PRESCRIPTION DRUG | NDA |
METHOTREXATE SODIUM | 59137-510-04 | Medexus Pharma Inc. | NDA205776 | HUMAN PRESCRIPTION DRUG | NDA |
METHOTREXATE SODIUM | 59651-182-36 | Aurobindo Pharma Limited | ANDA210454 | HUMAN PRESCRIPTION DRUG | ANDA |
METHOTREXATE SODIUM | 59137-515-01 | Medexus Pharma Inc. | NDA205776 | HUMAN PRESCRIPTION DRUG | NDA |
METHOTREXATE SODIUM | 71335-2221-1 | Bryant Ranch Prepack | ANDA210454 | HUMAN PRESCRIPTION DRUG | ANDA |
METHOTREXATE SODIUM | 0555-0572-02 | Teva Pharmaceuticals USA, Inc. | ANDA081099 | HUMAN PRESCRIPTION DRUG | ANDA |
METHOTREXATE SODIUM | 59137-510-01 | Medexus Pharma Inc. | NDA205776 | HUMAN PRESCRIPTION DRUG | NDA |
METHOTREXATE SODIUM | 59137-505-00 | Medexus Pharma Inc. | NDA205776 | HUMAN PRESCRIPTION DRUG | NDA |
METHOTREXATE SODIUM | 59137-505-04 | Medexus Pharma Inc. | NDA205776 | HUMAN PRESCRIPTION DRUG | NDA |
METHOTREXATE SODIUM | 51285-366-01 | Teva Women's Health, Inc. | ANDA040385 | HUMAN PRESCRIPTION DRUG | ANDA |
METHOTREXATE SODIUM | 61703-350-38 | Hospira, Inc. | NDA011719 | HUMAN PRESCRIPTION DRUG | NDA |
METHOTREXATE SODIUM | 21695-111-30 | Rebel Distributors Corp. | ANDA081099 | HUMAN PRESCRIPTION DRUG | ANDA |
METHOTREXATE SODIUM | 59137-550-00 | Medexus Pharma Inc. | NDA205776 | HUMAN PRESCRIPTION DRUG | NDA |
METHOTREXATE SODIUM | 16729-486-01 | Accord Healthcare Inc. | ANDA213343 | HUMAN PRESCRIPTION DRUG | ANDA |
METHOTREXATE SODIUM | 71335-2221-2 | Bryant Ranch Prepack | ANDA210454 | HUMAN PRESCRIPTION DRUG | ANDA |
METHOTREXATE SODIUM | 0054-8550-25 | Hikma Pharmaceuticals USA Inc. | ANDA040054 | HUMAN PRESCRIPTION DRUG | ANDA |
METHOTREXATE SODIUM | 71335-1772-7 | Bryant Ranch Prepack | ANDA213343 | HUMAN PRESCRIPTION DRUG | ANDA |
METHOTREXATE SODIUM | 61703-124-40 | Hospira, Inc. | NDA011719 | HUMAN PRESCRIPTION DRUG | NDA |
METHOTREXATE SODIUM | 42254-110-30 | Rebel Distributors Corp. | NDA008085 | HUMAN PRESCRIPTION DRUG | NDA |
METHOTREXATE SODIUM | 51407-121-01 | Golden State Medical Supply, Inc. | ANDA081235 | HUMAN PRESCRIPTION DRUG | ANDA |
METHOTREXATE SODIUM | 59137-515-00 | Medexus Pharma Inc. | NDA205776 | HUMAN PRESCRIPTION DRUG | NDA |
METHOTREXATE SODIUM | 71335-1772-5 | Bryant Ranch Prepack | ANDA213343 | HUMAN PRESCRIPTION DRUG | ANDA |
METHOTREXATE SODIUM | 71335-2221-6 | Bryant Ranch Prepack | ANDA210454 | HUMAN PRESCRIPTION DRUG | ANDA |
METHOTREXATE SODIUM | 70518-3263-2 | REMEDYREPACK INC. | ANDA213343 | HUMAN PRESCRIPTION DRUG | ANDA |
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