Package 72789-544-90

Brand: bupropion hydrochloride

Generic: bupropion hydrochloride
NDC Package

Package Facts

Identity

Package NDC 72789-544-90
Digits Only 7278954490
Product NDC 72789-544
Product ID 72789-544_47ac1ba1-8e8b-b872-e063-6394a90a5dbb
Description

90 TABLET in 1 BOTTLE, PLASTIC (72789-544-90)

Marketing

Marketing Status
Marketed Since 2026-01-05
Brand bupropion hydrochloride
Generic bupropion hydrochloride
Sample Package No

Linked Drug Pages (1)

bupropion Hydrochloride ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "47ac1ba1-8e8b-b872-e063-6394a90a5dbb", "openfda": {"upc": ["0372789544908"], "unii": ["ZG7E5POY8O"], "rxcui": ["993687"], "spl_set_id": ["90cc4f07-e0a3-4d50-a10a-8f6a7f9c5140"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE, PLASTIC (72789-544-90)", "package_ndc": "72789-544-90", "marketing_start_date": "20260105"}], "brand_name": "bupropion Hydrochloride", "product_id": "72789-544_47ac1ba1-8e8b-b872-e063-6394a90a5dbb", "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": "72789-544", "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": "ANDA206975", "marketing_category": "ANDA", "marketing_start_date": "20160819", "listing_expiration_date": "20271231"}