FDA NDC Directory · JSON-LD · Markdown

Methocarbamol

NDC 69584-612 · HUMAN PRESCRIPTION DRUG · TABLET

Generic namemethocarbamol
Labeler / ManufacturerOxford Pharmaceuticals, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA040489
Dosage form / routeTABLET · ORAL
Active ingredientsMETHOCARBAMOL (750 mg/1)
Marketing started20190815
Package count4

External sources

Source: openFDA. Public-domain (CC0).