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Methocarbamol

NDC 43547-226 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerSolco Healthcare LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA086988
Dosage form / routeTABLET · ORAL
Active ingredientsMETHOCARBAMOL (750 mg/1)
Marketing started20130115
Package count2

External sources

Source: openFDA. Public-domain (CC0).