FDA NDC Directory · JSON-LD · Markdown

METHADONE HYDROCHLORIDE

NDC 0054-0709 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerHikma Pharmaceuticals USA Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA088109
Dosage form / routeTABLET · ORAL
Active ingredientsMETHADONE HYDROCHLORIDE (5 mg/1)
Marketing started19830308
Package count2

External sources

Source: openFDA. Public-domain (CC0).