Package 71335-2312-6

Brand: bupropion hydrochloride (xl)

Generic: bupropion hydrochloride
NDC Package

Package Facts

Identity

Package NDC 71335-2312-6
Digits Only 7133523126
Product NDC 71335-2312
Description

180 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (71335-2312-6)

Marketing

Marketing Status
Marketed Since 2023-12-21
Brand bupropion hydrochloride (xl)
Generic bupropion hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "0de542bc-6bdc-426f-bfdd-e004fca8405c", "openfda": {"unii": ["ZG7E5POY8O"], "rxcui": ["993557"], "spl_set_id": ["8499470a-8d01-4348-b67b-8f49728031cb"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (71335-2312-1)", "package_ndc": "71335-2312-1", "marketing_start_date": "20231221"}, {"sample": false, "description": "60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (71335-2312-2)", "package_ndc": "71335-2312-2", "marketing_start_date": "20231221"}, {"sample": false, "description": "90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (71335-2312-3)", "package_ndc": "71335-2312-3", "marketing_start_date": "20231221"}, {"sample": false, "description": "120 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (71335-2312-4)", "package_ndc": "71335-2312-4", "marketing_start_date": "20231221"}, {"sample": false, "description": "8 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (71335-2312-5)", "package_ndc": "71335-2312-5", "marketing_start_date": "20231221"}, {"sample": false, "description": "180 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (71335-2312-6)", "package_ndc": "71335-2312-6", "marketing_start_date": "20231221"}], "brand_name": "Bupropion Hydrochloride (XL)", "product_id": "71335-2312_0de542bc-6bdc-426f-bfdd-e004fca8405c", "dosage_form": "TABLET, FILM COATED, EXTENDED RELEASE", "pharm_class": ["Aminoketone [EPC]", "Dopamine Uptake Inhibitors [MoA]", "Increased Dopamine Activity [PE]", "Increased Norepinephrine Activity [PE]", "Norepinephrine Uptake Inhibitors [MoA]"], "product_ndc": "71335-2312", "generic_name": "bupropion hydrochloride", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Bupropion Hydrochloride", "brand_name_suffix": "(XL)", "active_ingredients": [{"name": "BUPROPION HYDROCHLORIDE", "strength": "300 mg/1"}], "application_number": "ANDA207479", "marketing_category": "ANDA", "marketing_start_date": "20170412", "listing_expiration_date": "20261231"}