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Methotrexate

NDC 48433-065 · HUMAN PRESCRIPTION DRUG · TABLET

Generic namemethotrexate
Labeler / ManufacturerSafecor Health LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA081235
Dosage form / routeTABLET · ORAL
Active ingredientsMETHOTREXATE SODIUM (2.5 mg/1)
Marketing started20260119
Package count1

External sources

Source: openFDA. Public-domain (CC0).