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Midodrine Hydrochloride

NDC 82293-005 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerNovugen Pharma (USA) LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA211973
Dosage form / routeTABLET · ORAL
Active ingredientsMIDODRINE HYDROCHLORIDE (10 mg/1)
Marketing started20231018
Package count1

External sources

Source: openFDA. Public-domain (CC0).