FDA NDC Directory · JSON-LD · Markdown

Methocarbamol

NDC 82461-723 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerMedcore LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA212623
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsMETHOCARBAMOL (750 mg/1)
Marketing started20260731
Package count1

External sources

Source: openFDA. Public-domain (CC0).