Package 72162-1925-1

Brand: buspirone hydrochloride

Generic: buspirone hydrochloride
NDC Package

Package Facts

Identity

Package NDC 72162-1925-1
Digits Only 7216219251
Product NDC 72162-1925
Description

100 TABLET in 1 BOTTLE (72162-1925-1)

Marketing

Marketing Status
Marketed Since 2020-07-27
Brand buspirone hydrochloride
Generic buspirone hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "5c7d0f84-ca14-4aef-87aa-79f3c5b49270", "openfda": {"unii": ["207LT9J9OC"], "rxcui": ["866083"], "spl_set_id": ["aba814f0-55ce-4480-99f1-b9ad1ba77d3f"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (72162-1925-1)", "package_ndc": "72162-1925-1", "marketing_start_date": "20200727"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (72162-1925-5)", "package_ndc": "72162-1925-5", "marketing_start_date": "20200727"}], "brand_name": "Buspirone Hydrochloride", "product_id": "72162-1925_5c7d0f84-ca14-4aef-87aa-79f3c5b49270", "dosage_form": "TABLET", "product_ndc": "72162-1925", "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": "10 mg/1"}], "application_number": "ANDA075388", "marketing_category": "ANDA", "marketing_start_date": "20200727", "listing_expiration_date": "20261231"}