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MIDODRINE HYDROCHLORIDE

NDC 46708-339 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerAlembic Pharmaceuticals Limited
Marketing categoryAbbreviated NDA (generic) · App ANDA214734
Dosage form / routeTABLET · ORAL
Active ingredientsMIDODRINE HYDROCHLORIDE (5 mg/1)
Marketing started20210122
Package count2

External sources

Source: openFDA. Public-domain (CC0).