FDA NDC Directory · JSON-LD · Markdown

Methocarbamol Tablets, USP, 750 mg

NDC 63561-0174 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Generic nameMethocarbamol
Labeler / ManufacturerGranulation Technology, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA212623
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsMETHOCARBAMOL (750 mg/1)
Marketing started20250610
Package count2

External sources

Source: openFDA. Public-domain (CC0).