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Methocarbamol

NDC 68788-8172 · HUMAN PRESCRIPTION DRUG · TABLET, COATED

Generic nameMethocarbamol Tablets
Labeler / ManufacturerPreferred Pharmaceuticals Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA209312
Dosage form / routeTABLET, COATED · ORAL
Active ingredientsMETHOCARBAMOL (750 mg/1)
Marketing started20220425
Package count3

External sources

Source: openFDA. Public-domain (CC0).