Package 70518-4056-1

Brand: bupropion hydrochloride sr

Generic: bupropion hydrochloride
NDC Package

Package Facts

Identity

Package NDC 70518-4056-1
Digits Only 7051840561
Product NDC 70518-4056
Product ID 70518-4056_4c98ba8c-05d9-6c1d-e063-6394a90ab0d7
Description

30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (70518-4056-1)

Marketing

Marketing Status
Marketed Since 2025-01-23
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": "4c98ba8c-05d9-6c1d-e063-6394a90ab0d7", "openfda": {"unii": ["ZG7E5POY8O"], "rxcui": ["993518"], "spl_set_id": ["b47c5515-a438-40bc-b8ad-26a6cf9676b7"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (70518-4056-1)", "package_ndc": "70518-4056-1", "marketing_start_date": "20250123"}], "brand_name": "Bupropion Hydrochloride SR", "product_id": "70518-4056_4c98ba8c-05d9-6c1d-e063-6394a90ab0d7", "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": "70518-4056", "generic_name": "bupropion hydrochloride", "labeler_name": "REMEDYREPACK INC.", "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": "20240419", "listing_expiration_date": "20271231"}