Package 63629-2138-1

Brand: bupropion hydrochloride

Generic: bupropion hydrochloride
NDC Package

Package Facts

Identity

Package NDC 63629-2138-1
Digits Only 6362921381
Product NDC 63629-2138
Product ID 63629-2138_7e67f0e9-c8f1-40fd-b9cd-c08ca8f3f718
Description

500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (63629-2138-1)

Marketing

Marketing Status
Marketed Since 2007-06-12
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": "7e67f0e9-c8f1-40fd-b9cd-c08ca8f3f718", "openfda": {"unii": ["ZG7E5POY8O"], "rxcui": ["993557"], "spl_set_id": ["bd3f1706-e6e0-4db1-b09e-5e718976766a"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (63629-2138-1)", "package_ndc": "63629-2138-1", "marketing_start_date": "20070612"}], "brand_name": "Bupropion Hydrochloride", "product_id": "63629-2138_7e67f0e9-c8f1-40fd-b9cd-c08ca8f3f718", "dosage_form": "TABLET, FILM COATED, EXTENDED RELEASE", "pharm_class": ["Aminoketone [EPC]", "Dopamine Uptake Inhibitors [MoA]", "Increased Dopamine Activity [PE]", "Increased Norepinephrine Activity [PE]", "Norepinephrine Uptake Inhibitors [MoA]"], "product_ndc": "63629-2138", "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": "300 mg/1"}], "application_number": "ANDA077284", "marketing_category": "ANDA", "marketing_start_date": "20070612", "listing_expiration_date": "20261231"}