Package 70518-4448-0

Brand: bupropion hydrochloride

Generic: bupropion hydrochloride
NDC Package

Package Facts

Identity

Package NDC 70518-4448-0
Digits Only 7051844480
Product NDC 70518-4448
Product ID 70518-4448_3cb78452-65e0-c964-e063-6394a90a1c92
Description

30 TABLET in 1 BLISTER PACK (70518-4448-0)

Marketing

Marketing Status
Marketed Since 2025-08-19
Brand bupropion hydrochloride
Generic bupropion hydrochloride
Sample Package No

Linked Drug Pages (0)

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Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "3cb78452-65e0-c964-e063-6394a90a1c92", "openfda": {"unii": ["ZG7E5POY8O"], "rxcui": ["993541"], "spl_set_id": ["82872e51-3349-40fe-8ea3-496751955fed"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BLISTER PACK (70518-4448-0)", "package_ndc": "70518-4448-0", "marketing_start_date": "20250819"}], "brand_name": "Bupropion hydrochloride", "product_id": "70518-4448_3cb78452-65e0-c964-e063-6394a90a1c92", "dosage_form": "TABLET", "pharm_class": ["Aminoketone [EPC]", "Dopamine Uptake Inhibitors [MoA]", "Increased Dopamine Activity [PE]", "Increased Norepinephrine Activity [PE]", "Norepinephrine Uptake Inhibitors [MoA]"], "product_ndc": "70518-4448", "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": "20250819", "listing_expiration_date": "20261231"}