Package 70518-3279-0

Brand: buspirone hydrochloride

Generic: buspirone hydrochloride
NDC Package

Package Facts

Identity

Package NDC 70518-3279-0
Digits Only 7051832790
Product NDC 70518-3279
Product ID 70518-3279_3b8cff42-4e64-0e4d-e063-6294a90a0e2b
Description

30 TABLET in 1 BLISTER PACK (70518-3279-0)

Marketing

Marketing Status
Marketed Since 2021-11-30
Brand buspirone hydrochloride
Generic buspirone hydrochloride
Sample Package No

Linked Drug Pages (0)

No linked drugs yet.

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "3b8cff42-4e64-0e4d-e063-6294a90a0e2b", "openfda": {"unii": ["207LT9J9OC"], "rxcui": ["866083"], "spl_set_id": ["6c6db7a9-a728-406a-81af-edd89e1cc26f"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BLISTER PACK (70518-3279-0)", "package_ndc": "70518-3279-0", "marketing_start_date": "20211130"}, {"sample": false, "description": "30 TABLET in 1 BLISTER PACK (70518-3279-1)", "package_ndc": "70518-3279-1", "marketing_start_date": "20250731"}], "brand_name": "Buspirone Hydrochloride", "product_id": "70518-3279_3b8cff42-4e64-0e4d-e063-6294a90a0e2b", "dosage_form": "TABLET", "product_ndc": "70518-3279", "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": "ANDA210907", "marketing_category": "ANDA", "marketing_start_date": "20211130", "listing_expiration_date": "20261231"}