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Methocarbamol

NDC 0904-7057 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerMajor Pharmaceuticals
Marketing categoryAbbreviated NDA (generic) · App ANDA086988
Dosage form / routeTABLET · ORAL
Active ingredientsMETHOCARBAMOL (500 mg/1)
Marketing started20171215
Package count1

External sources

Source: openFDA. Public-domain (CC0).