Package 70518-1166-1

Brand: Buspirone hydrochloride

Generic: Buspirone hydrochloride
NDC Package

Package Facts

Identity

Package NDC 70518-1166-1
Digits Only 7051811661
Product NDC 70518-1166
Description

30 TABLET in 1 BLISTER PACK (70518-1166-1)

Marketing

Marketing Status
Marketed Since 2025-02-12
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": "48bfa14c-4b7c-6038-e063-6394a90a562d", "openfda": {"unii": ["207LT9J9OC"], "rxcui": ["866083"], "spl_set_id": ["a90c2dd6-3e95-407d-af05-ad2fbcc1fccd"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BLISTER PACK (70518-1166-1)", "package_ndc": "70518-1166-1", "marketing_start_date": "20250212"}], "brand_name": "Buspirone hydrochloride", "product_id": "70518-1166_48bfa14c-4b7c-6038-e063-6394a90a562d", "dosage_form": "TABLET", "product_ndc": "70518-1166", "generic_name": "Buspirone hydrochloride", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Buspirone hydrochloride", "active_ingredients": [{"name": "BUSPIRONE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA078888", "marketing_category": "ANDA", "marketing_start_date": "20180511", "listing_expiration_date": "20271231"}