Package 50268-135-15
Brand: buspirone hydrochloride
Generic: buspirone hydrochloridePackage Facts
Identity
Package NDC
50268-135-15
Digits Only
5026813515
Product NDC
50268-135
Description
50 BLISTER PACK in 1 BOX (50268-135-15) / 1 TABLET in 1 BLISTER PACK (50268-135-11)
Marketing
Marketing Status
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": "4c3657a8-f6bd-b2a4-e063-6394a90a741d", "openfda": {"unii": ["207LT9J9OC"], "rxcui": ["866018"], "spl_set_id": ["b230197c-3d50-7874-e053-2a95a90af50f"], "manufacturer_name": ["AvPAK"]}, "finished": true, "packaging": [{"sample": false, "description": "50 BLISTER PACK in 1 BOX (50268-135-15) / 1 TABLET in 1 BLISTER PACK (50268-135-11)", "package_ndc": "50268-135-15", "marketing_start_date": "20201021"}], "brand_name": "Buspirone hydrochloride", "product_id": "50268-135_4c3657a8-f6bd-b2a4-e063-6394a90a741d", "dosage_form": "TABLET", "product_ndc": "50268-135", "generic_name": "Buspirone hydrochloride", "labeler_name": "AvPAK", "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": "20201021", "listing_expiration_date": "20271231"}