Package 71335-2690-1

Brand: bupropion hydrochloride

Generic: bupropion hydrochloride
NDC Package

Package Facts

Identity

Package NDC 71335-2690-1
Digits Only 7133526901
Product NDC 71335-2690
Product ID 71335-2690_5b646edc-1c51-4ba5-8d18-1c9c32dd47fb
Description

100 TABLET in 1 BOTTLE (71335-2690-1)

Marketing

Marketing Status
Marketed Since 2025-06-30
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": "5b646edc-1c51-4ba5-8d18-1c9c32dd47fb", "openfda": {"unii": ["ZG7E5POY8O"], "rxcui": ["993687"], "spl_set_id": ["744f7394-aac9-4864-9436-e5b0b35a6148"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (71335-2690-1)", "package_ndc": "71335-2690-1", "marketing_start_date": "20250630"}], "brand_name": "bupropion Hydrochloride", "product_id": "71335-2690_5b646edc-1c51-4ba5-8d18-1c9c32dd47fb", "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": "71335-2690", "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"}