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Midodrine Hydrochloride

NDC 71205-905 · HUMAN PRESCRIPTION DRUG · TABLET

Generic namemidodrine hydrochloride
Labeler / ManufacturerProficient Rx LP
Marketing categoryAbbreviated NDA (generic) · App ANDA207849
Dosage form / routeTABLET · ORAL
Active ingredientsMIDODRINE HYDROCHLORIDE (5 mg/1)
Marketing started20201015
Package count7

External sources

Source: openFDA. Public-domain (CC0).