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Midodrine Hydrochloride

NDC 23155-970 · HUMAN PRESCRIPTION DRUG · TABLET

Generic namemidodrine hydrochloride
Labeler / ManufacturerAvet Pharmaceuticals Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA076725
Dosage form / routeTABLET · ORAL
Active ingredientsMIDODRINE HYDROCHLORIDE (5 mg/1)
Marketing started20260325
Package count1

External sources

Source: openFDA. Public-domain (CC0).