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Midodrine Hydrochloride

NDC 60505-1325 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerApotex Corp
Marketing categoryAbbreviated NDA (generic) · App ANDA077746
Dosage form / routeTABLET · ORAL
Active ingredientsMIDODRINE HYDROCHLORIDE (10 mg/1)
Marketing started20060912
Package count4

External sources

Source: openFDA. Public-domain (CC0).