FDA NDC Directory · JSON-LD · Markdown

Methotrexate Sodium

NDC 64850-330 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerElite Laboratories, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA216453
Dosage form / routeTABLET · ORAL
Active ingredientsMETHOTREXATE SODIUM (2.5 mg/1)
Marketing started20240516
Package count1

External sources

Source: openFDA. Public-domain (CC0).