FDA NDC Directory · JSON-LD · Markdown

METHOCARBAMOL

NDC 61919-368 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerDIRECT RX
Marketing categoryAbbreviated NDA (generic) · App ANDA090200
Dosage form / routeTABLET · ORAL
Active ingredientsMETHOCARBAMOL (500 mg/1)
Marketing started20190418
Package count5

External sources

Source: openFDA. Public-domain (CC0).