FDA NDC Directory · JSON-LD · Markdown

Methotrexate

NDC 68071-3991 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerNuCare Pharmaceuticals, Inc.
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).