# Buspirone hydrochloride

NDC: 68382-181
Generic name: Buspirone hydrochloride
Labeler / Manufacturer: Zydus Pharmaceuticals USA Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20140503

FDA application: ANDA078888

## Active ingredients

- BUSPIRONE HYDROCHLORIDE: 10 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"68382-181"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=68382-181
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=14fd7c1c-778e-46d4-9024-89b319f15f39