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Mirabegron

NDC 69238-2861 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED, EXTENDED RELEASE

Labeler / ManufacturerAmneal Pharmaceuticals NY LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA218543
Dosage form / routeTABLET, FILM COATED, EXTENDED RELEASE · ORAL
Active ingredientsMIRABEGRON (50 mg/1)
Marketing started20260419
Package count2

External sources

Source: openFDA. Public-domain (CC0).