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Pramipexole dihydrochloride

NDC 55111-613 · HUMAN PRESCRIPTION DRUG · TABLET, EXTENDED RELEASE

Labeler / ManufacturerDr. Reddy's Laboratories Limited
Marketing categoryAbbreviated NDA (generic) · App ANDA203354
Dosage form / routeTABLET, EXTENDED RELEASE · ORAL
Active ingredientsPRAMIPEXOLE DIHYDROCHLORIDE (1.5 mg/1)
Marketing started20150814
Package count1

External sources

Source: openFDA. Public-domain (CC0).