Package 72162-1924-5

Brand: buspirone hydrochloride

Generic: buspirone hydrochloride
NDC Package

Package Facts

Identity

Package NDC 72162-1924-5
Digits Only 7216219245
Product NDC 72162-1924
Product ID 72162-1924_90144727-e59d-4a04-a880-3258d52c869e
Description

500 TABLET in 1 BOTTLE (72162-1924-5)

Marketing

Marketing Status
Marketed Since 2024-01-31
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": "90144727-e59d-4a04-a880-3258d52c869e", "openfda": {"unii": ["207LT9J9OC"], "rxcui": ["866094"], "spl_set_id": ["bee0edbf-3fc3-484b-9715-f13a329216ae"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (72162-1924-1)", "package_ndc": "72162-1924-1", "marketing_start_date": "20240131"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (72162-1924-5)", "package_ndc": "72162-1924-5", "marketing_start_date": "20240131"}], "brand_name": "Buspirone Hydrochloride", "product_id": "72162-1924_90144727-e59d-4a04-a880-3258d52c869e", "dosage_form": "TABLET", "product_ndc": "72162-1924", "generic_name": "buspirone hydrochloride", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Buspirone Hydrochloride", "active_ingredients": [{"name": "BUSPIRONE HYDROCHLORIDE", "strength": "5 mg/1"}], "application_number": "ANDA075388", "marketing_category": "ANDA", "marketing_start_date": "20200727", "listing_expiration_date": "20261231"}