Package 50090-6872-0

Brand: bupropion hydrochloride sr

Generic: bupropion hydrochloride
NDC Package

Package Facts

Identity

Package NDC 50090-6872-0
Digits Only 5009068720
Product NDC 50090-6872
Product ID 50090-6872_5324a48e-2adc-4cb7-a84e-b8b4ead410a5
Description

90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (50090-6872-0)

Marketing

Marketing Status
Marketed Since 2023-12-04
Brand bupropion hydrochloride sr
Generic bupropion hydrochloride
Sample Package No

Linked Drug Pages (1)

Bupropion Hydrochloride SR ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "5324a48e-2adc-4cb7-a84e-b8b4ead410a5", "openfda": {"unii": ["ZG7E5POY8O"], "rxcui": ["993518"], "spl_set_id": ["339c7157-1c65-40d1-bbcc-c10348d908d3"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (50090-6872-0)", "package_ndc": "50090-6872-0", "marketing_start_date": "20231204"}], "brand_name": "Bupropion Hydrochloride SR", "product_id": "50090-6872_5324a48e-2adc-4cb7-a84e-b8b4ead410a5", "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": "50090-6872", "generic_name": "bupropion hydrochloride", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Bupropion Hydrochloride", "brand_name_suffix": "SR", "active_ingredients": [{"name": "BUPROPION HYDROCHLORIDE", "strength": "150 mg/1"}], "application_number": "ANDA205794", "marketing_category": "ANDA", "marketing_start_date": "20180420", "listing_expiration_date": "20261231"}