Package 63629-2414-1

Brand: buspirone hydrochloride

Generic: buspirone hydrochloride
NDC Package

Package Facts

Identity

Package NDC 63629-2414-1
Digits Only 6362924141
Product NDC 63629-2414
Product ID 63629-2414_f8962a3c-fd6d-4241-bcf1-4f42b419d9b6
Description

500 TABLET in 1 BOTTLE (63629-2414-1)

Marketing

Marketing Status
Marketed Since 2021-02-24
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": "f8962a3c-fd6d-4241-bcf1-4f42b419d9b6", "openfda": {"unii": ["207LT9J9OC"], "rxcui": ["866090"], "spl_set_id": ["8bb7991e-ab09-4602-b49d-0a72a501685b"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "500 TABLET in 1 BOTTLE (63629-2414-1)", "package_ndc": "63629-2414-1", "marketing_start_date": "20210224"}], "brand_name": "Buspirone Hydrochloride", "product_id": "63629-2414_f8962a3c-fd6d-4241-bcf1-4f42b419d9b6", "dosage_form": "TABLET", "product_ndc": "63629-2414", "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"}