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Pramipexole Dihydrochloride Extended-Release

NDC 69680-145 · HUMAN PRESCRIPTION DRUG · TABLET, EXTENDED RELEASE

Generic namePramipexole Dihydrochloride
Labeler / ManufacturerVitruvias Therapeutics, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA212797
Dosage form / routeTABLET, EXTENDED RELEASE · ORAL
Active ingredientsPRAMIPEXOLE DIHYDROCHLORIDE (.375 mg/1)
Marketing started20210827
Package count1

External sources

Source: openFDA. Public-domain (CC0).