bupropion hydrochloride

Generic: bupropion hydrochloride

Labeler: pd-rx pharmaceuticals, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name bupropion hydrochloride
Generic Name bupropion hydrochloride
Labeler pd-rx pharmaceuticals, inc.
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

bupropion hydrochloride 75 mg/1

Manufacturer
PD-Rx Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 43063-880
Product ID 43063-880_3a216a96-02f5-5996-e063-6294a90a187d
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 43063880
Hyphenated Format 43063-880

Supplemental Identifiers

RxCUI
993691
UPC
0343063880302
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
  • 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-880-30)
  • 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-880-60)
source: ndc

Packages (2)

43063-880-30 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-880-30) 43063-880-60 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-880-60)

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": "3a216a96-02f5-5996-e063-6294a90a187d", "openfda": {"upc": ["0343063880302"], "unii": ["ZG7E5POY8O"], "rxcui": ["993691"], "spl_set_id": ["b5c12c9a-62eb-481a-8099-7ad35242f7bf"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-880-30)", "package_ndc": "43063-880-30", "marketing_start_date": "20180813"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-880-60)", "package_ndc": "43063-880-60", "marketing_start_date": "20181030"}], "brand_name": "Bupropion Hydrochloride", "product_id": "43063-880_3a216a96-02f5-5996-e063-6294a90a187d", "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": "43063-880", "generic_name": "Bupropion Hydrochloride", "labeler_name": "PD-Rx Pharmaceuticals, Inc.", "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"}