Package 68071-3559-9

Brand: bupropion hydrochloride

Generic: bupropion hydrochloride
NDC Package

Package Facts

Identity

Package NDC 68071-3559-9
Digits Only 6807135599
Product NDC 68071-3559
Product ID 68071-3559_2ad12986-97e7-b958-e063-6294a90ad875
Description

90 TABLET, EXTENDED RELEASE in 1 BOTTLE (68071-3559-9)

Marketing

Marketing Status
Marketed Since 2024-01-09
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": "2ad12986-97e7-b958-e063-6294a90ad875", "openfda": {"upc": ["0368071355994"], "unii": ["ZG7E5POY8O"], "rxcui": ["993541"], "spl_set_id": ["0e8b2109-8516-2d92-e063-6394a90a5d16"], "manufacturer_name": ["NuCare Pharmaceuticals,Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, EXTENDED RELEASE in 1 BOTTLE (68071-3559-9)", "package_ndc": "68071-3559-9", "marketing_start_date": "20240109"}], "brand_name": "Bupropion Hydrochloride", "product_id": "68071-3559_2ad12986-97e7-b958-e063-6294a90ad875", "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": "68071-3559", "generic_name": "Bupropion Hydrochloride", "labeler_name": "NuCare Pharmaceuticals,Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Bupropion Hydrochloride", "active_ingredients": [{"name": "BUPROPION HYDROCHLORIDE", "strength": "150 mg/1"}], "application_number": "ANDA090693", "marketing_category": "ANDA", "marketing_start_date": "20170614", "listing_expiration_date": "20261231"}