FDA NDC Directory · JSON-LD · Markdown

Methotrexate

NDC 60687-975 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerAmerican Health Packaging
Marketing categoryAbbreviated NDA (generic) · App ANDA207812
Dosage form / routeTABLET · ORAL
Active ingredientsMETHOTREXATE (2.5 mg/1)
Marketing started20261001
Package count1

External sources

Source: openFDA. Public-domain (CC0).