Package 72162-2097-1

Brand: bupropion hydrochloride

Generic: bupropion hydrochloride
NDC Package

Package Facts

Identity

Package NDC 72162-2097-1
Digits Only 7216220971
Product NDC 72162-2097
Product ID 72162-2097_f63dcf38-c7a9-4861-86ec-e8a0fffd29ef
Description

100 TABLET, FILM COATED in 1 BOTTLE (72162-2097-1)

Marketing

Marketing Status
Marketed Since 2006-01-17
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": "f63dcf38-c7a9-4861-86ec-e8a0fffd29ef", "openfda": {"unii": ["ZG7E5POY8O"], "rxcui": ["993687"], "spl_set_id": ["fa5fa0d8-d27f-44e1-8868-dfa7206524e2"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (72162-2097-1)", "package_ndc": "72162-2097-1", "marketing_start_date": "20060117"}], "brand_name": "Bupropion Hydrochloride", "product_id": "72162-2097_f63dcf38-c7a9-4861-86ec-e8a0fffd29ef", "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": "72162-2097", "generic_name": "Bupropion Hydrochloride", "labeler_name": "Bryant Ranch Prepack", "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"}