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Methocarbamol

NDC 76420-258 · HUMAN PRESCRIPTION DRUG · TABLET

Generic namemethocarbamol
Labeler / ManufacturerAsclemed USA, Inc.
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).