# Buspirone hydrochloride

NDC: 77771-235
Generic name: Buspirone hydrochloride
Labeler / Manufacturer: Radha Pharmaceuticals, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20250918

FDA application: ANDA202087

## Active ingredients

- BUSPIRONE HYDROCHLORIDE: 7.5 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"77771-235"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=77771-235
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=3f66a3fe-9d73-180c-e063-6394a90aacca