Package 71335-0013-2

Brand: bupropion hydrochloride

Generic: bupropion hydrochloride
NDC Package

Package Facts

Identity

Package NDC 71335-0013-2
Digits Only 7133500132
Product NDC 71335-0013
Description

60 TABLET, FILM COATED in 1 BOTTLE (71335-0013-2)

Marketing

Marketing Status
Marketed Since 2018-02-21
Brand bupropion hydrochloride
Generic bupropion hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "c9822446-5f21-4d08-983a-226b3557f18d", "openfda": {"unii": ["ZG7E5POY8O"], "rxcui": ["993691"], "spl_set_id": ["1d722dc2-7909-454e-b989-095677079044"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (71335-0013-1)", "package_ndc": "71335-0013-1", "marketing_start_date": "20180308"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (71335-0013-2)", "package_ndc": "71335-0013-2", "marketing_start_date": "20180221"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (71335-0013-3)", "package_ndc": "71335-0013-3", "marketing_start_date": "20240709"}, {"sample": false, "description": "7 TABLET, FILM COATED in 1 BOTTLE (71335-0013-4)", "package_ndc": "71335-0013-4", "marketing_start_date": "20240709"}, {"sample": false, "description": "14 TABLET, FILM COATED in 1 BOTTLE (71335-0013-5)", "package_ndc": "71335-0013-5", "marketing_start_date": "20240709"}, {"sample": false, "description": "120 TABLET, FILM COATED in 1 BOTTLE (71335-0013-6)", "package_ndc": "71335-0013-6", "marketing_start_date": "20240709"}, {"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (71335-0013-7)", "package_ndc": "71335-0013-7", "marketing_start_date": "20240709"}], "brand_name": "Bupropion Hydrochloride", "product_id": "71335-0013_c9822446-5f21-4d08-983a-226b3557f18d", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Aminoketone [EPC]", "Dopamine Uptake Inhibitors [MoA]", "Increased Dopamine Activity [PE]", "Increased Norepinephrine Activity [PE]", "Norepinephrine Uptake Inhibitors [MoA]"], "product_ndc": "71335-0013", "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": "75 mg/1"}], "application_number": "ANDA076143", "marketing_category": "ANDA", "marketing_start_date": "20060117", "listing_expiration_date": "20261231"}