Package 70518-2987-0

Brand: buspirone hydrochloride

Generic: buspirone hydrochloride
NDC Package

Package Facts

Identity

Package NDC 70518-2987-0
Digits Only 7051829870
Product NDC 70518-2987
Product ID 70518-2987_4af2d002-47c4-b68f-e063-6294a90af7c1
Description

30 TABLET in 1 BLISTER PACK (70518-2987-0)

Marketing

Marketing Status
Marketed Since 2021-01-12
Brand buspirone hydrochloride
Generic buspirone hydrochloride
Sample Package No

Linked Drug Pages (1)

Buspirone Hydrochloride ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "4af2d002-47c4-b68f-e063-6294a90af7c1", "openfda": {"unii": ["207LT9J9OC"], "rxcui": ["866018"], "spl_set_id": ["3155e607-bc7f-4e90-9edf-8e862dd5737d"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BLISTER PACK (70518-2987-0)", "package_ndc": "70518-2987-0", "marketing_start_date": "20210112"}, {"sample": false, "description": "60 TABLET in 1 BLISTER PACK (70518-2987-2)", "package_ndc": "70518-2987-2", "marketing_start_date": "20250712"}], "brand_name": "Buspirone Hydrochloride", "product_id": "70518-2987_4af2d002-47c4-b68f-e063-6294a90af7c1", "dosage_form": "TABLET", "product_ndc": "70518-2987", "generic_name": "buspirone hydrochloride", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Buspirone Hydrochloride", "active_ingredients": [{"name": "BUSPIRONE HYDROCHLORIDE", "strength": "15 mg/1"}], "application_number": "ANDA075388", "marketing_category": "ANDA", "marketing_start_date": "20210112", "listing_expiration_date": "20271231"}