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Midodrine Hydrochloride

NDC 72162-2559 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerBryant Ranch Prepack
Marketing categoryAbbreviated NDA (generic) · App ANDA212774
Dosage form / routeTABLET · ORAL
Active ingredientsMIDODRINE HYDROCHLORIDE (10 mg/1)
Marketing started20200810
Package count1

External sources

Source: openFDA. Public-domain (CC0).