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Pramipexole Dihydrochloride

NDC 50090-2455 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerA-S Medication Solutions
Marketing categoryAbbreviated NDA (generic) · App ANDA202633
Dosage form / routeTABLET · ORAL
Active ingredientsPRAMIPEXOLE DIHYDROCHLORIDE (.5 mg/1)
Marketing started20121026
Package count1

External sources

Source: openFDA. Public-domain (CC0).