Package 0904-7121-61

Brand: buspirone hydrochloride

Generic: buspirone hydrochloride
NDC Package

Package Facts

Identity

Package NDC 0904-7121-61
Digits Only 0904712161
Product NDC 0904-7121
Product ID 0904-7121_7e3f9aeb-2fcc-4f4d-921b-a4b96a932d19
Description

100 BLISTER PACK in 1 CARTON (0904-7121-61) / 1 TABLET in 1 BLISTER PACK

Marketing

Marketing Status
Marketed Since 2012-06-29
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": "7e3f9aeb-2fcc-4f4d-921b-a4b96a932d19", "openfda": {"unii": ["207LT9J9OC"], "rxcui": ["866083", "866094"], "spl_set_id": ["8dc1ee33-e5aa-4462-8fb9-9bbdf5463488"], "manufacturer_name": ["Major Pharmaceuticals"]}, "finished": true, "packaging": [{"sample": false, "description": "100 BLISTER PACK in 1 CARTON (0904-7121-61)  / 1 TABLET in 1 BLISTER PACK", "package_ndc": "0904-7121-61", "marketing_start_date": "20120629"}], "brand_name": "Buspirone Hydrochloride", "product_id": "0904-7121_7e3f9aeb-2fcc-4f4d-921b-a4b96a932d19", "dosage_form": "TABLET", "product_ndc": "0904-7121", "generic_name": "Buspirone Hydrochloride", "labeler_name": "Major Pharmaceuticals", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Buspirone Hydrochloride", "active_ingredients": [{"name": "BUSPIRONE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA204582", "marketing_category": "ANDA", "marketing_start_date": "20120629", "listing_expiration_date": "20261231"}