FDA NDC Directory · JSON-LD · Markdown

Methadone Hydrochloride

NDC 67877-660 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerAscend Laboratories, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA090635
Dosage form / routeTABLET · ORAL
Active ingredientsMETHADONE HYDROCHLORIDE (10 mg/1)
Marketing started20250701
Package count1

External sources

Source: openFDA. Public-domain (CC0).