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Pramipexole Dihydrochloride

NDC 65862-604 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerAurobindo Pharma Limited
Marketing categoryAbbreviated NDA (generic) · App ANDA202633
Dosage form / routeTABLET · ORAL
Active ingredientsPRAMIPEXOLE DIHYDROCHLORIDE (.125 mg/1)
Marketing started20121026
Package count3

External sources

Source: openFDA. Public-domain (CC0).