Package 72162-1927-5

Brand: buspirone hydrochloride

Generic: buspirone hydrochloride
NDC Package

Package Facts

Identity

Package NDC 72162-1927-5
Digits Only 7216219275
Product NDC 72162-1927
Product ID 72162-1927_c2768d6f-ba1c-418a-a565-63fcd6b6bce9
Description

500 TABLET in 1 BOTTLE (72162-1927-5)

Marketing

Marketing Status
Marketed Since 2020-05-01
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": "c2768d6f-ba1c-418a-a565-63fcd6b6bce9", "openfda": {"unii": ["207LT9J9OC"], "rxcui": ["866090"], "spl_set_id": ["eb072818-3ca8-430b-91a1-e7fedd37990c"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "500 TABLET in 1 BOTTLE (72162-1927-5)", "package_ndc": "72162-1927-5", "marketing_start_date": "20200501"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (72162-1927-6)", "package_ndc": "72162-1927-6", "marketing_start_date": "20200501"}], "brand_name": "Buspirone Hydrochloride", "product_id": "72162-1927_c2768d6f-ba1c-418a-a565-63fcd6b6bce9", "dosage_form": "TABLET", "product_ndc": "72162-1927", "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": "30 mg/1"}], "application_number": "ANDA078302", "marketing_category": "ANDA", "marketing_start_date": "20200501", "listing_expiration_date": "20261231"}