Package 71335-2875-1

Brand: bupropion hydrochloride

Generic: bupropion hydrochloride
NDC Package

Package Facts

Identity

Package NDC 71335-2875-1
Digits Only 7133528751
Product NDC 71335-2875
Product ID 71335-2875_cd607962-0181-41ca-89a1-b719ef13656b
Description

100 TABLET in 1 BOTTLE (71335-2875-1)

Marketing

Marketing Status
Marketed Since 2025-10-22
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": "cd607962-0181-41ca-89a1-b719ef13656b", "openfda": {"unii": ["ZG7E5POY8O"], "rxcui": ["993687"], "spl_set_id": ["e2a988f2-f8d3-4de0-b9f1-49d8c2e4180f"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (71335-2875-1)", "package_ndc": "71335-2875-1", "marketing_start_date": "20251022"}], "brand_name": "bupropion Hydrochloride", "product_id": "71335-2875_cd607962-0181-41ca-89a1-b719ef13656b", "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": "71335-2875", "generic_name": "bupropion Hydrochloride", "labeler_name": "Bryant Ranch Prepack", "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": "20160819", "listing_expiration_date": "20261231"}