Package 70518-4068-0

Brand: buspirone hydrochloride

Generic: buspirone hydrochloride
NDC Package

Package Facts

Identity

Package NDC 70518-4068-0
Digits Only 7051840680
Product NDC 70518-4068
Product ID 70518-4068_3fa2e69e-0c7d-9409-e063-6394a90a7ccc
Description

30 TABLET in 1 BLISTER PACK (70518-4068-0)

Marketing

Marketing Status
Marketed Since 2024-05-05
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": "3fa2e69e-0c7d-9409-e063-6394a90a7ccc", "openfda": {"unii": ["207LT9J9OC"], "rxcui": ["866090"], "spl_set_id": ["ed2b56fe-e02f-46bc-808a-352f9bbb5b57"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BLISTER PACK (70518-4068-0)", "package_ndc": "70518-4068-0", "marketing_start_date": "20240505"}], "brand_name": "Buspirone Hydrochloride", "product_id": "70518-4068_3fa2e69e-0c7d-9409-e063-6394a90a7ccc", "dosage_form": "TABLET", "product_ndc": "70518-4068", "generic_name": "Buspirone Hydrochloride", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Buspirone Hydrochloride", "active_ingredients": [{"name": "BUSPIRONE HYDROCHLORIDE", "strength": "30 mg/1"}], "application_number": "ANDA210907", "marketing_category": "ANDA", "marketing_start_date": "20240505", "listing_expiration_date": "20261231"}