bupropion hydrochloride

Generic: bupropion hydrochloride

Labeler: cardinal health 107, llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name bupropion hydrochloride
Generic Name bupropion hydrochloride
Labeler cardinal health 107, llc
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

bupropion hydrochloride 75 mg/1

Manufacturer
Cardinal Health 107, LLC

Identifiers & Regulatory

Product NDC 55154-4152
Product ID 55154-4152_11bc1544-6f4a-4ada-90e0-1c3ae28205b8
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA076143
Listing Expiration 2026-12-31
Marketing Start 2006-01-17

Pharmacologic Class

Classes
aminoketone [epc] dopamine uptake inhibitors [moa] increased dopamine activity [pe] increased norepinephrine activity [pe] norepinephrine uptake inhibitors [moa]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 551544152
Hyphenated Format 55154-4152

Supplemental Identifiers

RxCUI
993691
UPC
0055154415200
UNII
ZG7E5POY8O

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name bupropion hydrochloride (source: ndc)
Generic Name bupropion hydrochloride (source: ndc)
Application Number ANDA076143 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 75 mg/1
source: ndc
Packaging
  • 10 BLISTER PACK in 1 BAG (55154-4152-0) / 1 TABLET, FILM COATED in 1 BLISTER PACK
source: ndc

Packages (1)

55154-4152-0 10 BLISTER PACK in 1 BAG (55154-4152-0) / 1 TABLET, FILM COATED in 1 BLISTER PACK

Ingredients (1)

bupropion hydrochloride (75 mg/1)

Linked Drug Pages (1)

Bupropion Hydrochloride ndc-match (0.9)

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"}