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Aripiprazole

NDC 67046-1085 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerCoupler LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA202101
Dosage form / routeTABLET · ORAL
Active ingredientsARIPIPRAZOLE (20 mg/1)
Marketing started20260527
Package count1

External sources

Source: openFDA. Public-domain (CC0).