FDA NDC Directory · JSON-LD · Markdown

Metoprolol Tartrate

NDC 68071-3723 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerNuCare Pharmaceuticals, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA200981
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsMETOPROLOL TARTRATE (25 mg/1)
Marketing started20181201
Package count3

External sources

Source: openFDA. Public-domain (CC0).