Package 70518-4052-0

Brand: buspirone hydrochloride

Generic: buspirone hydrochloride
NDC Package

Package Facts

Identity

Package NDC 70518-4052-0
Digits Only 7051840520
Product NDC 70518-4052
Description

30 TABLET in 1 BLISTER PACK (70518-4052-0)

Marketing

Marketing Status
Marketed Since 2024-04-15
Brand buspirone hydrochloride
Generic buspirone hydrochloride
Sample Package No

Linked Drug Pages (0)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "44ac71c4-0d57-7cc2-e063-6294a90abb89", "openfda": {"unii": ["207LT9J9OC"], "rxcui": ["866018"], "spl_set_id": ["fbff8248-b73c-474e-907e-449f8316c629"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BLISTER PACK (70518-4052-0)", "package_ndc": "70518-4052-0", "marketing_start_date": "20240415"}, {"sample": false, "description": "30 TABLET in 1 BLISTER PACK (70518-4052-2)", "package_ndc": "70518-4052-2", "marketing_start_date": "20250212"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE, PLASTIC (70518-4052-3)", "package_ndc": "70518-4052-3", "marketing_start_date": "20250618"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE, PLASTIC (70518-4052-4)", "package_ndc": "70518-4052-4", "marketing_start_date": "20251128"}], "brand_name": "Buspirone Hydrochloride", "product_id": "70518-4052_44ac71c4-0d57-7cc2-e063-6294a90abb89", "dosage_form": "TABLET", "product_ndc": "70518-4052", "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": "ANDA210907", "marketing_category": "ANDA", "marketing_start_date": "20240415", "listing_expiration_date": "20261231"}