Package 60429-746-01

Brand: bupropion hydrochloride

Generic: bupropion hydrochloride
NDC Package

Package Facts

Identity

Package NDC 60429-746-01
Digits Only 6042974601
Product NDC 60429-746
Description

100 TABLET, FILM COATED in 1 BOTTLE (60429-746-01)

Marketing

Marketing Status
Marketed Since 2019-08-22
Brand bupropion hydrochloride
Generic bupropion hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "43e78c36-28fa-06c3-e063-6394a90a221b", "openfda": {"unii": ["ZG7E5POY8O"], "rxcui": ["993687", "993691"], "spl_set_id": ["9490d611-b679-45c7-e053-2a95a90afb87"], "manufacturer_name": ["Golden State Medical Supply, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (60429-746-01)", "package_ndc": "60429-746-01", "marketing_start_date": "20190822"}], "brand_name": "Bupropion Hydrochloride", "product_id": "60429-746_43e78c36-28fa-06c3-e063-6394a90a221b", "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": "60429-746", "generic_name": "Bupropion Hydrochloride", "labeler_name": "Golden State Medical Supply, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Bupropion Hydrochloride", "active_ingredients": [{"name": "BUPROPION HYDROCHLORIDE", "strength": "75 mg/1"}], "application_number": "ANDA076143", "marketing_category": "ANDA", "marketing_start_date": "20060117", "listing_expiration_date": "20261231"}