FDA NDC Directory · JSON-LD · Markdown

MEPROBAMATE

NDC 46708-019 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerAlembic Pharmaceuticals Limited
Marketing categoryAbbreviated NDA (generic) · App ANDA090122
Dosage form / routeTABLET · ORAL
Active ingredientsMEPROBAMATE (200 mg/1)
Marketing started20130723
Package count3

External sources

Source: openFDA. Public-domain (CC0).