FDA NDC Directory · JSON-LD · Markdown

Buspirone Hydrochloride

NDC 69584-094 · HUMAN PRESCRIPTION DRUG · TABLET

Generic namebuspirone hydrochloride
Labeler / ManufacturerOxford Pharmaceuticals, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA078302
Dosage form / routeTABLET · ORAL
Active ingredientsBUSPIRONE HYDROCHLORIDE (30 mg/1)
Marketing started20200501
Package count3

External sources

Source: openFDA. Public-domain (CC0).