Package 63187-766-90

Brand: bupropion hydrochloride xl

Generic: bupropion hydrochloride
NDC Package

Package Facts

Identity

Package NDC 63187-766-90
Digits Only 6318776690
Product NDC 63187-766
Product ID 63187-766_42428c55-bb9b-44be-a82f-478f6d22500d
Description

90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (63187-766-90)

Marketing

Marketing Status
Marketed Since 2016-11-01
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": "42428c55-bb9b-44be-a82f-478f6d22500d", "openfda": {"upc": ["0363187766900"], "unii": ["ZG7E5POY8O"], "rxcui": ["993541"], "spl_set_id": ["ec9cbb38-1582-492f-a526-4b3675c55b14"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (63187-766-30)", "package_ndc": "63187-766-30", "marketing_start_date": "20161101"}, {"sample": false, "description": "60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (63187-766-60)", "package_ndc": "63187-766-60", "marketing_start_date": "20161101"}, {"sample": false, "description": "90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (63187-766-90)", "package_ndc": "63187-766-90", "marketing_start_date": "20161101"}], "brand_name": "Bupropion Hydrochloride XL", "product_id": "63187-766_42428c55-bb9b-44be-a82f-478f6d22500d", "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": "63187-766", "generic_name": "Bupropion Hydrochloride", "labeler_name": "Proficient Rx LP", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Bupropion Hydrochloride", "brand_name_suffix": "XL", "active_ingredients": [{"name": "BUPROPION HYDROCHLORIDE", "strength": "150 mg/1"}], "application_number": "ANDA077715", "marketing_category": "ANDA", "marketing_start_date": "20081126", "listing_expiration_date": "20261231"}