Package 71610-975-60

Brand: buspirone hydrochloride

Generic: buspirone hydrochloride
NDC Package

Package Facts

Identity

Package NDC 71610-975-60
Digits Only 7161097560
Product NDC 71610-975
Description

90 TABLET in 1 BOTTLE (71610-975-60)

Marketing

Marketing Status
Marketed Since 2025-12-12
Brand buspirone hydrochloride
Generic buspirone hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "45c63c90-30a3-54ff-e063-6394a90af15f", "openfda": {"unii": ["207LT9J9OC"], "rxcui": ["866018"], "spl_set_id": ["45c637b7-3057-ea38-e063-6394a90a87b6"], "manufacturer_name": ["Aphena Pharma Solutions - Tennessee, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE (71610-975-60)", "package_ndc": "71610-975-60", "marketing_start_date": "20251212"}], "brand_name": "Buspirone hydrochloride", "product_id": "71610-975_45c63c90-30a3-54ff-e063-6394a90af15f", "dosage_form": "TABLET", "product_ndc": "71610-975", "generic_name": "Buspirone hydrochloride", "labeler_name": "Aphena Pharma Solutions - Tennessee, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Buspirone hydrochloride", "active_ingredients": [{"name": "BUSPIRONE HYDROCHLORIDE", "strength": "15 mg/1"}], "application_number": "ANDA202087", "marketing_category": "ANDA", "marketing_start_date": "20250918", "listing_expiration_date": "20261231"}