Package 0904-6899-61

Brand: buspirone hydrochloride

Generic: buspirone hydrochloride
NDC Package

Package Facts

Identity

Package NDC 0904-6899-61
Digits Only 0904689961
Product NDC 0904-6899
Description

100 BLISTER PACK in 1 CARTON (0904-6899-61) / 1 TABLET in 1 BLISTER PACK

Marketing

Marketing Status
Marketed Since 2014-05-03
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": "88587ddd-72d8-4312-8619-e78e2393cdb6", "openfda": {"unii": ["207LT9J9OC"], "rxcui": ["866018"], "spl_set_id": ["a9bb9216-3dac-4e8a-9df9-f72c2eaef160"], "manufacturer_name": ["Major Pharmaceuticals"]}, "finished": true, "packaging": [{"sample": false, "description": "100 BLISTER PACK in 1 CARTON (0904-6899-61)  / 1 TABLET in 1 BLISTER PACK", "package_ndc": "0904-6899-61", "marketing_start_date": "20140503"}], "brand_name": "Buspirone hydrochloride", "product_id": "0904-6899_88587ddd-72d8-4312-8619-e78e2393cdb6", "dosage_form": "TABLET", "product_ndc": "0904-6899", "generic_name": "Buspirone hydrochloride", "labeler_name": "Major Pharmaceuticals", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Buspirone hydrochloride", "active_ingredients": [{"name": "BUSPIRONE HYDROCHLORIDE", "strength": "15 mg/1"}], "application_number": "ANDA078888", "marketing_category": "ANDA", "marketing_start_date": "20140503", "listing_expiration_date": "20261231"}