FDA NDC Directory · JSON-LD · Markdown

Methocarbamol

NDC 60687-568 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerAmerican Health Packaging
Marketing categoryAbbreviated NDA (generic) · App ANDA090200
Dosage form / routeTABLET · ORAL
Active ingredientsMETHOCARBAMOL (750 mg/1)
Marketing started20200520
Package count1

External sources

Source: openFDA. Public-domain (CC0).