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Metoprolol Succinate

NDC 27808-305 · HUMAN PRESCRIPTION DRUG · TABLET, EXTENDED RELEASE

Labeler / ManufacturerCranbury Pharmaceuticals, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA207206
Dosage form / routeTABLET, EXTENDED RELEASE · ORAL
Active ingredientsMETOPROLOL SUCCINATE (200 mg/1)
Marketing started20250601
Package count1

External sources

Source: openFDA. Public-domain (CC0).