Package 82804-123-30

Brand: bupropion hydrochloride

Generic: bupropion hydrochloride
NDC Package

Package Facts

Identity

Package NDC 82804-123-30
Digits Only 8280412330
Product NDC 82804-123
Product ID 82804-123_13560bf8-eb25-44f0-968e-db70d51219af
Description

30 TABLET, FILM COATED in 1 BOTTLE (82804-123-30)

Marketing

Marketing Status
Marketed Since 2024-07-15
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": "13560bf8-eb25-44f0-968e-db70d51219af", "openfda": {"upc": ["0382804123308", "0382804127306"], "unii": ["ZG7E5POY8O"], "rxcui": ["993687", "993691"], "spl_set_id": ["13560bf8-eb25-44f0-968e-db70d51219af"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (82804-123-30)", "package_ndc": "82804-123-30", "marketing_start_date": "20240715"}], "brand_name": "Bupropion Hydrochloride", "product_id": "82804-123_13560bf8-eb25-44f0-968e-db70d51219af", "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": "82804-123", "generic_name": "Bupropion Hydrochloride", "labeler_name": "Proficient Rx LP", "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"}