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Methocarbamol

NDC 72789-021 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerPD-Rx Pharmaceuticals, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA208507
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsMETHOCARBAMOL (500 mg/1)
Marketing started20180115
Package count7

External sources

Source: openFDA. Public-domain (CC0).