# Buspirone hydrochloride

NDC: 42806-665
Generic name: Buspirone hydrochloride
Labeler / Manufacturer: EPIC PHARMA, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20200619

FDA application: ANDA202087

## Active ingredients

- BUSPIRONE HYDROCHLORIDE: 30 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"42806-665"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=42806-665
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=e8f43c66-f8de-419f-9ea9-43ddc4ec0798