Package 72516-036-09

Brand: bupropion hydrochloride xl

Generic: bupropion hydrochloride
NDC Package

Package Facts

Identity

Package NDC 72516-036-09
Digits Only 7251603609
Product NDC 72516-036
Product ID 72516-036_47afeb95-a677-8969-e063-6294a90a7b2d
Description

90 TABLET, EXTENDED RELEASE in 1 BOTTLE (72516-036-09)

Marketing

Marketing Status
Marketed Since 2019-09-06
Brand bupropion hydrochloride xl
Generic bupropion hydrochloride
Sample Package No

Linked Drug Pages (1)

buPropion Hydrochloride XL ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "47afeb95-a677-8969-e063-6294a90a7b2d", "openfda": {"upc": ["0372516036096", "0372516036508", "0372516035037", "0372516035099", "0372516035501", "0372516036034"], "unii": ["ZG7E5POY8O"], "rxcui": ["993541", "993557"], "spl_set_id": ["004d8121-59d4-46c4-acb8-b2dd097bf556"], "manufacturer_name": ["Oryza pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, EXTENDED RELEASE in 1 BOTTLE (72516-036-03)", "package_ndc": "72516-036-03", "marketing_start_date": "20190906"}, {"sample": false, "description": "90 TABLET, EXTENDED RELEASE in 1 BOTTLE (72516-036-09)", "package_ndc": "72516-036-09", "marketing_start_date": "20190906"}, {"sample": false, "description": "500 TABLET, EXTENDED RELEASE in 1 BOTTLE (72516-036-50)", "package_ndc": "72516-036-50", "marketing_start_date": "20190906"}], "brand_name": "buPropion Hydrochloride XL", "product_id": "72516-036_47afeb95-a677-8969-e063-6294a90a7b2d", "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": "72516-036", "generic_name": "bupropion hydrochloride", "labeler_name": "Oryza pharmaceuticals Inc.", "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": "ANDA211200", "marketing_category": "ANDA", "marketing_start_date": "20190906", "listing_expiration_date": "20271231"}