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METHOTREXATE

NDC 62332-712 · HUMAN PRESCRIPTION DRUG · INJECTION, SOLUTION

Generic namemethotrexate
Labeler / ManufacturerAlembic Pharmaceuticals Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA220225
Dosage form / routeINJECTION, SOLUTION · INTRAMUSCULAR INTRATHECAL INTRAVENOUS SUBCUTANEOUS
Active ingredientsMETHOTREXATE SODIUM (25 mg/mL)
Marketing started20260415
Package count1

External sources

Source: openFDA. Public-domain (CC0).