Package 70518-4189-0

Brand: bupropion hydrochloride

Generic: bupropion hydrochloride
NDC Package

Package Facts

Identity

Package NDC 70518-4189-0
Digits Only 7051841890
Product NDC 70518-4189
Product ID 70518-4189_3ff2feab-69af-b316-e063-6294a90a6509
Description

30 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (70518-4189-0)

Marketing

Marketing Status
Marketed Since 2024-09-26
Brand bupropion hydrochloride
Generic bupropion hydrochloride
Sample Package No

Linked Drug Pages (0)

No linked drugs yet.

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "3ff2feab-69af-b316-e063-6294a90a6509", "openfda": {"unii": ["ZG7E5POY8O"], "rxcui": ["993541"], "spl_set_id": ["c60855ca-4fa0-4004-ad19-4abb61100c43"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (70518-4189-0)", "package_ndc": "70518-4189-0", "marketing_start_date": "20240926"}], "brand_name": "Bupropion hydrochloride", "product_id": "70518-4189_3ff2feab-69af-b316-e063-6294a90a6509", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Aminoketone [EPC]", "Dopamine Uptake Inhibitors [MoA]", "Increased Dopamine Activity [PE]", "Increased Norepinephrine Activity [PE]", "Norepinephrine Uptake Inhibitors [MoA]"], "product_ndc": "70518-4189", "generic_name": "Bupropion hydrochloride", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Bupropion hydrochloride", "active_ingredients": [{"name": "BUPROPION HYDROCHLORIDE", "strength": "150 mg/1"}], "application_number": "ANDA215568", "marketing_category": "ANDA", "marketing_start_date": "20240926", "listing_expiration_date": "20261231"}