Package 70518-2031-5

Brand: buspirone hydrochloride

Generic: buspirone hydrochloride
NDC Package

Package Facts

Identity

Package NDC 70518-2031-5
Digits Only 7051820315
Product NDC 70518-2031
Product ID 70518-2031_499b44fe-d3dc-219a-e063-6294a90a0428
Description

90 TABLET in 1 BOTTLE, PLASTIC (70518-2031-5)

Marketing

Marketing Status
Marketed Since 2025-06-30
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": "499b44fe-d3dc-219a-e063-6294a90a0428", "openfda": {"unii": ["207LT9J9OC"], "rxcui": ["866083"], "spl_set_id": ["a9fc7091-b3ce-45fd-8d89-aeebdd81c327"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET in 1 BOTTLE, PLASTIC (70518-2031-4)", "package_ndc": "70518-2031-4", "marketing_start_date": "20250618"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE, PLASTIC (70518-2031-5)", "package_ndc": "70518-2031-5", "marketing_start_date": "20250630"}], "brand_name": "Buspirone Hydrochloride", "product_id": "70518-2031_499b44fe-d3dc-219a-e063-6294a90a0428", "dosage_form": "TABLET", "product_ndc": "70518-2031", "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": "ANDA204582", "marketing_category": "ANDA", "marketing_start_date": "20190418", "listing_expiration_date": "20271231"}