Package 71335-1214-6

Brand: bupropion hydrochloride

Generic: bupropion hydrochloride
NDC Package

Package Facts

Identity

Package NDC 71335-1214-6
Digits Only 7133512146
Product NDC 71335-1214
Description

180 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1214-6)

Marketing

Marketing Status
Marketed Since 2024-08-09
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": "4e5c9883-8fbd-443f-a356-b0793cd27687", "openfda": {"unii": ["ZG7E5POY8O"], "rxcui": ["993557"], "spl_set_id": ["82bcdd72-9146-4c8d-a8aa-f92015864605"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1214-1)", "package_ndc": "71335-1214-1", "marketing_start_date": "20190503"}, {"sample": false, "description": "60 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1214-2)", "package_ndc": "71335-1214-2", "marketing_start_date": "20210422"}, {"sample": false, "description": "90 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1214-3)", "package_ndc": "71335-1214-3", "marketing_start_date": "20190610"}, {"sample": false, "description": "120 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1214-4)", "package_ndc": "71335-1214-4", "marketing_start_date": "20190529"}, {"sample": false, "description": "8 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1214-5)", "package_ndc": "71335-1214-5", "marketing_start_date": "20240809"}, {"sample": false, "description": "180 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1214-6)", "package_ndc": "71335-1214-6", "marketing_start_date": "20240809"}], "brand_name": "BUPROPION HYDROCHLORIDE", "product_id": "71335-1214_4e5c9883-8fbd-443f-a356-b0793cd27687", "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": "71335-1214", "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": "300 mg/1"}], "application_number": "ANDA210497", "marketing_category": "ANDA", "marketing_start_date": "20190325", "listing_expiration_date": "20261231"}