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Methocarbamol Tablets, USP, 500 mg

NDC 72789-481 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Generic nameMethocarbamol
Labeler / ManufacturerPD-Rx Pharmaceuticals, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA212623
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsMETHOCARBAMOL (500 mg/1)
Marketing started20250610
Package count7

External sources

Source: openFDA. Public-domain (CC0).