# Buspirone Hydrochloride

NDC: 68788-7952
Generic name: Buspirone Hydrochloride
Labeler / Manufacturer: Preferred Pharmaceuticals Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20210709

FDA application: ANDA210907

## Active ingredients

- BUSPIRONE HYDROCHLORIDE: 5 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"68788-7952"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=68788-7952
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=824c80e6-d508-405f-8a4f-2f10df5a9dc8