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Aripiprazole

NDC 46708-255 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerAlembic Pharmaceuticals Limited
Marketing categoryAbbreviated NDA (generic) · App ANDA202101
Dosage form / routeTABLET · ORAL
Active ingredientsARIPIPRAZOLE (5 mg/1)
Marketing started20150428
Package count7

External sources

Source: openFDA. Public-domain (CC0).