Package 55154-4152-0
Brand: bupropion hydrochloride
Generic: bupropion hydrochloridePackage Facts
Identity
Package NDC
55154-4152-0
Digits Only
5515441520
Product NDC
55154-4152
Description
10 BLISTER PACK in 1 BAG (55154-4152-0) / 1 TABLET, FILM COATED in 1 BLISTER PACK
Marketing
Marketing Status
Brand
bupropion hydrochloride
Generic
bupropion hydrochloride
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "11bc1544-6f4a-4ada-90e0-1c3ae28205b8", "openfda": {"upc": ["0055154415200"], "unii": ["ZG7E5POY8O"], "rxcui": ["993691"], "spl_set_id": ["ec4d2256-0340-4166-90ee-c264eef3ac82"], "manufacturer_name": ["Cardinal Health 107, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "10 BLISTER PACK in 1 BAG (55154-4152-0) / 1 TABLET, FILM COATED in 1 BLISTER PACK", "package_ndc": "55154-4152-0", "marketing_start_date": "20220518"}], "brand_name": "Bupropion Hydrochloride", "product_id": "55154-4152_11bc1544-6f4a-4ada-90e0-1c3ae28205b8", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Aminoketone [EPC]", "Dopamine Uptake Inhibitors [MoA]", "Increased Dopamine Activity [PE]", "Increased Norepinephrine Activity [PE]", "Norepinephrine Uptake Inhibitors [MoA]"], "product_ndc": "55154-4152", "generic_name": "Bupropion Hydrochloride", "labeler_name": "Cardinal Health 107, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Bupropion Hydrochloride", "active_ingredients": [{"name": "BUPROPION HYDROCHLORIDE", "strength": "75 mg/1"}], "application_number": "ANDA076143", "marketing_category": "ANDA", "marketing_start_date": "20060117", "listing_expiration_date": "20261231"}