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Buspirone Hydrochloride

NDC 70518-4586 · HUMAN PRESCRIPTION DRUG · TABLET

Generic namebuspirone hydrochloride
Labeler / ManufacturerREMEDYREPACK INC.
Marketing categoryAbbreviated NDA (generic) · App ANDA075388
Dosage form / routeTABLET · ORAL
Active ingredientsBUSPIRONE HYDROCHLORIDE (5 mg/1)
Marketing started20260319
Package count1

External sources

Source: openFDA. Public-domain (CC0).