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BUSPIRONE HYDROCHLORIDE

NDC 59651-389 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerAurobindo Pharma Limited
Marketing categoryAbbreviated NDA (generic) · App ANDA078246
Dosage form / routeTABLET · ORAL
Active ingredientsBUSPIRONE HYDROCHLORIDE (5 mg/1)
Marketing started20200221
Package count5

External sources

Source: openFDA. Public-domain (CC0).