Package 42806-662-05

Brand: buspirone hydrochloride

Generic: buspirone hydrochloride
NDC Package

Package Facts

Identity

Package NDC 42806-662-05
Digits Only 4280666205
Product NDC 42806-662
Description

500 TABLET in 1 BOTTLE (42806-662-05)

Marketing

Marketing Status
Marketed Since 2020-06-19
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": "ac140e7e-3d5b-4329-8e3e-e21be7417fed", "openfda": {"unii": ["207LT9J9OC"], "rxcui": ["866018", "866083", "866090", "866094"], "spl_set_id": ["e8f43c66-f8de-419f-9ea9-43ddc4ec0798"], "manufacturer_name": ["EPIC PHARMA, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (42806-662-01)", "package_ndc": "42806-662-01", "marketing_start_date": "20200619"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (42806-662-05)", "package_ndc": "42806-662-05", "marketing_start_date": "20200619"}], "brand_name": "Buspirone hydrochloride", "product_id": "42806-662_ac140e7e-3d5b-4329-8e3e-e21be7417fed", "dosage_form": "TABLET", "product_ndc": "42806-662", "generic_name": "Buspirone hydrochloride", "labeler_name": "EPIC PHARMA, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Buspirone hydrochloride", "active_ingredients": [{"name": "BUSPIRONE HYDROCHLORIDE", "strength": "5 mg/1"}], "application_number": "ANDA202087", "marketing_category": "ANDA", "marketing_start_date": "20200619", "listing_expiration_date": "20261231"}