Package 67046-1562-3

Brand: bupropion hydrochloride

Generic: bupropion hydrochloride
NDC Package

Package Facts

Identity

Package NDC 67046-1562-3
Digits Only 6704615623
Product NDC 67046-1562
Product ID 67046-1562_35a871dc-a6ca-9963-e063-6294a90a4396
Description

30 TABLET in 1 BLISTER PACK (67046-1562-3)

Marketing

Marketing Status
Marketed Since 2025-05-21
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": "35a871dc-a6ca-9963-e063-6294a90a4396", "openfda": {"unii": ["ZG7E5POY8O"], "rxcui": ["993687"], "spl_set_id": ["35a873c5-4aa8-b3c7-e063-6394a90a35ec"], "manufacturer_name": ["Coupler LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BLISTER PACK (67046-1562-3)", "package_ndc": "67046-1562-3", "marketing_start_date": "20250521"}], "brand_name": "Bupropion Hydrochloride", "product_id": "67046-1562_35a871dc-a6ca-9963-e063-6294a90a4396", "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": "67046-1562", "generic_name": "Bupropion Hydrochloride", "labeler_name": "Coupler LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Bupropion Hydrochloride", "active_ingredients": [{"name": "BUPROPION HYDROCHLORIDE", "strength": "100 mg/1"}], "application_number": "ANDA206975", "marketing_category": "ANDA", "marketing_start_date": "20250521", "listing_expiration_date": "20261231"}