bupropion hydrochloride

Generic: bupropion hydrochloride

Labeler: heritage pharmaceuticals inc. d/b/a avet pharmaceuticals inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name bupropion hydrochloride
Generic Name bupropion hydrochloride
Labeler heritage pharmaceuticals inc. d/b/a avet pharmaceuticals inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

bupropion hydrochloride 100 mg/1

Manufacturer
Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.

Identifiers & Regulatory

Product NDC 23155-192
Product ID 23155-192_b72f6124-e8e4-42b7-8095-771ff429e936
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA206975
Listing Expiration 2026-12-31
Marketing Start 2016-08-19

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 23155192
Hyphenated Format 23155-192

Supplemental Identifiers

RxCUI
993687 993691
UPC
0323155191011 0323155192018
UNII
ZG7E5POY8O

Packaging Origin

Original Packager
true

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 ANDA206975 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 100 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (23155-192-01)
  • 1000 TABLET in 1 BOTTLE (23155-192-10)
source: ndc

Packages (2)

23155-192-01 100 TABLET in 1 BOTTLE (23155-192-01) 23155-192-10 1000 TABLET in 1 BOTTLE (23155-192-10)

Ingredients (1)

bupropion hydrochloride (100 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": "b72f6124-e8e4-42b7-8095-771ff429e936", "openfda": {"upc": ["0323155191011", "0323155192018"], "unii": ["ZG7E5POY8O"], "rxcui": ["993687", "993691"], "spl_set_id": ["9196568e-aec8-4d56-993e-4cbb78d4a3a6"], "manufacturer_name": ["Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (23155-192-01)", "package_ndc": "23155-192-01", "marketing_start_date": "20160819"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (23155-192-10)", "package_ndc": "23155-192-10", "marketing_start_date": "20160819"}], "brand_name": "bupropion Hydrochloride", "product_id": "23155-192_b72f6124-e8e4-42b7-8095-771ff429e936", "dosage_form": "TABLET", "pharm_class": ["Aminoketone [EPC]", "Dopamine Uptake Inhibitors [MoA]", "Increased Dopamine Activity [PE]", "Increased Norepinephrine Activity [PE]", "Norepinephrine Uptake Inhibitors [MoA]"], "product_ndc": "23155-192", "generic_name": "bupropion Hydrochloride", "labeler_name": "Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "bupropion Hydrochloride", "active_ingredients": [{"name": "BUPROPION HYDROCHLORIDE", "strength": "100 mg/1"}], "application_number": "ANDA206975", "marketing_category": "ANDA", "marketing_start_date": "20160819", "listing_expiration_date": "20261231"}