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Methotrexate

NDC 82804-136 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerProficient Rx LP
Marketing categoryAbbreviated NDA (generic) · App ANDA213343
Dosage form / routeTABLET · ORAL
Active ingredientsMETHOTREXATE SODIUM (2.5 mg/1)
Marketing started20200824
Package count1

External sources

Source: openFDA. Public-domain (CC0).