Package 70518-3906-0

Brand: buspirone hydrochloride

Generic: buspirone hydrochloride
NDC Package

Package Facts

Identity

Package NDC 70518-3906-0
Digits Only 7051839060
Product NDC 70518-3906
Product ID 70518-3906_3f8e5042-7595-3d55-e063-6294a90a4e4e
Description

30 TABLET in 1 BLISTER PACK (70518-3906-0)

Marketing

Marketing Status
Marketed Since 2023-11-03
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": "3f8e5042-7595-3d55-e063-6294a90a4e4e", "openfda": {"unii": ["207LT9J9OC"], "rxcui": ["866111"], "spl_set_id": ["fa3f9c0e-261d-4ceb-8cc7-e5e013563479"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BLISTER PACK (70518-3906-0)", "package_ndc": "70518-3906-0", "marketing_start_date": "20231103"}], "brand_name": "Buspirone hydrochloride", "product_id": "70518-3906_3f8e5042-7595-3d55-e063-6294a90a4e4e", "dosage_form": "TABLET", "product_ndc": "70518-3906", "generic_name": "Buspirone hydrochloride", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Buspirone hydrochloride", "active_ingredients": [{"name": "BUSPIRONE HYDROCHLORIDE", "strength": "7.5 mg/1"}], "application_number": "ANDA078888", "marketing_category": "ANDA", "marketing_start_date": "20231103", "listing_expiration_date": "20261231"}