Package 70518-0682-0

Brand: buspirone hydrochloride

Generic: buspirone hydrochloride
NDC Package

Package Facts

Identity

Package NDC 70518-0682-0
Digits Only 7051806820
Product NDC 70518-0682
Product ID 70518-0682_47fb4ce6-787a-6467-e063-6294a90ace55
Description

30 TABLET in 1 BLISTER PACK (70518-0682-0)

Marketing

Marketing Status
Marketed Since 2017-08-16
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": "47fb4ce6-787a-6467-e063-6294a90ace55", "openfda": {"unii": ["207LT9J9OC"], "rxcui": ["866094"], "spl_set_id": ["b42cc365-6259-4d2e-9648-d37718b65e1e"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BLISTER PACK (70518-0682-0)", "package_ndc": "70518-0682-0", "marketing_start_date": "20170816"}], "brand_name": "Buspirone Hydrochloride", "product_id": "70518-0682_47fb4ce6-787a-6467-e063-6294a90ace55", "dosage_form": "TABLET", "product_ndc": "70518-0682", "generic_name": "Buspirone Hydrochloride", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Buspirone Hydrochloride", "active_ingredients": [{"name": "BUSPIRONE HYDROCHLORIDE", "strength": "5 mg/1"}], "application_number": "ANDA202330", "marketing_category": "ANDA", "marketing_start_date": "20170816", "listing_expiration_date": "20271231"}