bupropion hydrochloride

Generic: bupropion hydrochloride

Labeler: coupler llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

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

bupropion hydrochloride 75 mg/1

Manufacturer
Coupler LLC

Identifiers & Regulatory

Product NDC 67046-1641
Product ID 67046-1641_47b96885-2003-29c2-e063-6294a90a2a35
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA075491
Listing Expiration 2027-12-31
Marketing Start 2026-01-06

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 670461641
Hyphenated Format 67046-1641

Supplemental Identifiers

RxCUI
993691
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 ANDA075491 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 75 mg/1
source: ndc
Packaging
  • 30 TABLET, FILM COATED in 1 BLISTER PACK (67046-1641-3)
source: ndc

Packages (1)

67046-1641-3 30 TABLET, FILM COATED in 1 BLISTER PACK (67046-1641-3)

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": "47b96885-2003-29c2-e063-6294a90a2a35", "openfda": {"unii": ["ZG7E5POY8O"], "rxcui": ["993691"], "spl_set_id": ["47b96919-a8ea-b769-e063-6394a90aa34e"], "manufacturer_name": ["Coupler LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BLISTER PACK (67046-1641-3)", "package_ndc": "67046-1641-3", "marketing_start_date": "20260106"}], "brand_name": "BUPROPION HYDROCHLORIDE", "product_id": "67046-1641_47b96885-2003-29c2-e063-6294a90a2a35", "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": "67046-1641", "generic_name": "BUPROPION HYDROCHLORIDE", "labeler_name": "Coupler LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "BUPROPION HYDROCHLORIDE", "active_ingredients": [{"name": "BUPROPION HYDROCHLORIDE", "strength": "75 mg/1"}], "application_number": "ANDA075491", "marketing_category": "ANDA", "marketing_start_date": "20260106", "listing_expiration_date": "20271231"}