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Midodrine hydrochloride

NDC 70771-1597 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerZydus Lifesciences Limited
Marketing categoryAbbreviated NDA (generic) · App ANDA213055
Dosage form / routeTABLET · ORAL
Active ingredientsMIDODRINE HYDROCHLORIDE (10 mg/1)
Marketing started20200917
Package count1

External sources

Source: openFDA. Public-domain (CC0).