Package 68071-3881-6

Brand: buspirone hydrochloride

Generic: buspirone hydrochloride
NDC Package

Package Facts

Identity

Package NDC 68071-3881-6
Digits Only 6807138816
Product NDC 68071-3881
Description

60 TABLET in 1 BOTTLE (68071-3881-6)

Marketing

Marketing Status
Marketed Since 2025-07-31
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": "3b4200bf-b66d-6936-e063-6394a90a6f19", "openfda": {"upc": ["0368071388169"], "unii": ["207LT9J9OC"], "rxcui": ["866083"], "spl_set_id": ["3b41fd76-c3cc-77f0-e063-6294a90aa778"], "manufacturer_name": ["NuCare Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET in 1 BOTTLE (68071-3881-6)", "package_ndc": "68071-3881-6", "marketing_start_date": "20250731"}], "brand_name": "Buspirone Hydrochloride", "product_id": "68071-3881_3b4200bf-b66d-6936-e063-6394a90a6f19", "dosage_form": "TABLET", "product_ndc": "68071-3881", "generic_name": "Buspirone Hydrochloride", "labeler_name": "NuCare Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Buspirone Hydrochloride", "active_ingredients": [{"name": "BUSPIRONE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA075022", "marketing_category": "ANDA", "marketing_start_date": "20020228", "listing_expiration_date": "20261231"}