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 100 mg/1

Manufacturer
PD-Rx Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 72789-070
Product ID 72789-070_3ca55d80-dd83-16fb-e063-6294a90afa4b
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 72789070
Hyphenated Format 72789-070

Supplemental Identifiers

RxCUI
993687
UPC
0372789070902
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
  • 100 mg/1
source: ndc
Packaging
  • 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-070-30)
  • 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-070-90)
source: ndc

Packages (2)

72789-070-30 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-070-30) 72789-070-90 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-070-90)

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": "3ca55d80-dd83-16fb-e063-6294a90afa4b", "openfda": {"upc": ["0372789070902"], "unii": ["ZG7E5POY8O"], "rxcui": ["993687"], "spl_set_id": ["867d3876-6974-4e89-bc45-9e60e84b401c"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-070-30)", "package_ndc": "72789-070-30", "marketing_start_date": "20200326"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-070-90)", "package_ndc": "72789-070-90", "marketing_start_date": "20240607"}], "brand_name": "Bupropion Hydrochloride", "product_id": "72789-070_3ca55d80-dd83-16fb-e063-6294a90afa4b", "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": "72789-070", "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": "100 mg/1"}], "application_number": "ANDA076143", "marketing_category": "ANDA", "marketing_start_date": "20060117", "listing_expiration_date": "20261231"}