FDA NDC Directory · JSON-LD · Markdown

Buspirone hydrochloride

NDC 68382-623 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerZydus Pharmaceuticals USA Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA078888
Dosage form / routeTABLET · ORAL
Active ingredientsBUSPIRONE HYDROCHLORIDE (7.5 mg/1)
Marketing started20230321
Package count4

External sources

Source: openFDA. Public-domain (CC0).