FDA NDC Directory · JSON-LD · Markdown

metoprolol succinate

NDC 51655-519 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED, EXTENDED RELEASE

Labeler / ManufacturerNorthwind Health Company, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA204161
Dosage form / routeTABLET, FILM COATED, EXTENDED RELEASE · ORAL
Active ingredientsMETOPROLOL SUCCINATE (50 mg/1)
Marketing started20221219
Package count2

External sources

Source: openFDA. Public-domain (CC0).