Package 42571-242-01

Brand: bupropion hydrochloride

Generic: bupropion hydrochloride
NDC Package

Package Facts

Identity

Package NDC 42571-242-01
Digits Only 4257124201
Product NDC 42571-242
Product ID 42571-242_42fa8097-2060-e261-e063-6294a90a6c29
Description

100 TABLET, FILM COATED in 1 BOTTLE (42571-242-01)

Marketing

Marketing Status
Marketed Since 2020-07-01
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": "42fa8097-2060-e261-e063-6294a90a6c29", "openfda": {"upc": ["0342571241018", "0342571242015"], "unii": ["ZG7E5POY8O"], "rxcui": ["993687", "993691"], "spl_set_id": ["03450d2d-97ce-4518-af15-ab85b0d65d76"], "manufacturer_name": ["Micro Labs Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (42571-242-01)", "package_ndc": "42571-242-01", "marketing_start_date": "20200701"}], "brand_name": "BUPROPION HYDROCHLORIDE", "product_id": "42571-242_42fa8097-2060-e261-e063-6294a90a6c29", "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": "42571-242", "generic_name": "Bupropion Hydrochloride", "labeler_name": "Micro Labs Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "BUPROPION HYDROCHLORIDE", "active_ingredients": [{"name": "BUPROPION HYDROCHLORIDE", "strength": "100 mg/1"}], "application_number": "ANDA207403", "marketing_category": "ANDA", "marketing_start_date": "20200701", "listing_expiration_date": "20261231"}