Package 70518-4317-0

Brand: buspirone hydrochloride

Generic: buspirone hydrochloride
NDC Package

Package Facts

Identity

Package NDC 70518-4317-0
Digits Only 7051843170
Product NDC 70518-4317
Product ID 70518-4317_3cf8b3b5-b4d8-216c-e063-6294a90a5156
Description

30 TABLET in 1 BLISTER PACK (70518-4317-0)

Marketing

Marketing Status
Marketed Since 2025-03-21
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": "3cf8b3b5-b4d8-216c-e063-6294a90a5156", "openfda": {"unii": ["207LT9J9OC"], "rxcui": ["866111"], "spl_set_id": ["fa4d5cac-f687-4440-99d2-8bb27cf2f4ed"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BLISTER PACK (70518-4317-0)", "package_ndc": "70518-4317-0", "marketing_start_date": "20250321"}], "brand_name": "BUSPIRONE HYDROCHLORIDE", "product_id": "70518-4317_3cf8b3b5-b4d8-216c-e063-6294a90a5156", "dosage_form": "TABLET", "product_ndc": "70518-4317", "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": "ANDA078246", "marketing_category": "ANDA", "marketing_start_date": "20250321", "listing_expiration_date": "20261231"}