FDA NDC Directory · JSON-LD · Markdown

Methocarbamol

NDC 70868-901 · HUMAN PRESCRIPTION DRUG · TABLET

Generic namemethocarbamol
Labeler / ManufacturerKey Therapeutics
Marketing categoryAbbreviated NDA (generic) · App ANDA040489
Dosage form / routeTABLET · ORAL
Active ingredientsMETHOCARBAMOL (750 mg/1)
Marketing started20191226
Package count1

External sources

Source: openFDA. Public-domain (CC0).