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Meprobamate

NDC 62332-020 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerAlembic Pharmaceuticals Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA090122
Dosage form / routeTABLET · ORAL
Active ingredientsMEPROBAMATE (400 mg/1)
Marketing started20160331
Package count3

External sources

Source: openFDA. Public-domain (CC0).