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MIRABEGRON

NDC 70518-4665 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED, EXTENDED RELEASE

Generic namemirabegron
Labeler / ManufacturerREMEDYREPACK INC.
Marketing categoryAbbreviated NDA (generic) · App ANDA209485
Dosage form / routeTABLET, FILM COATED, EXTENDED RELEASE · ORAL
Active ingredientsMIRABEGRON (50 mg/1)
Marketing started20260522
Package count1

External sources

Source: openFDA. Public-domain (CC0).