Package 71205-799-30

Brand: buspirone hydrochloride

Generic: buspirone hydrochloride
NDC Package

Package Facts

Identity

Package NDC 71205-799-30
Digits Only 7120579930
Product NDC 71205-799
Description

30 TABLET in 1 BOTTLE (71205-799-30)

Marketing

Marketing Status
Marketed Since 2023-05-05
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": "864ddd0c-80e5-4b4b-84e9-7d66214464ae", "openfda": {"upc": ["0371205799601"], "unii": ["207LT9J9OC"], "rxcui": ["866094"], "spl_set_id": ["864ddd0c-80e5-4b4b-84e9-7d66214464ae"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (71205-799-30)", "package_ndc": "71205-799-30", "marketing_start_date": "20230505"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (71205-799-60)", "package_ndc": "71205-799-60", "marketing_start_date": "20230505"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (71205-799-90)", "package_ndc": "71205-799-90", "marketing_start_date": "20230505"}], "brand_name": "Buspirone Hydrochloride", "product_id": "71205-799_864ddd0c-80e5-4b4b-84e9-7d66214464ae", "dosage_form": "TABLET", "product_ndc": "71205-799", "generic_name": "Buspirone Hydrochloride", "labeler_name": "Proficient Rx LP", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Buspirone Hydrochloride", "active_ingredients": [{"name": "BUSPIRONE HYDROCHLORIDE", "strength": "5 mg/1"}], "application_number": "ANDA075022", "marketing_category": "ANDA", "marketing_start_date": "20020228", "listing_expiration_date": "20261231"}