FDA NDC Directory · JSON-LD · Markdown

Methocarbamol

NDC 61919-616 · HUMAN PRESCRIPTION DRUG · TABLET, COATED

Labeler / ManufacturerDIRECT RX
Marketing categoryAbbreviated NDA (generic) · App ANDA209312
Dosage form / routeTABLET, COATED · ORAL
Active ingredientsMETHOCARBAMOL (750 mg/1)
Marketing started20190418
Package count3

External sources

Source: openFDA. Public-domain (CC0).