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Buspirone hydrochloride

NDC 67046-1352 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerCoupler LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA078888
Dosage form / routeTABLET · ORAL
Active ingredientsBUSPIRONE HYDROCHLORIDE (7.5 mg/1)
Marketing started20260610
Package count1

External sources

Source: openFDA. Public-domain (CC0).