Package 82804-064-90

Brand: ezetimibe

Generic: ezetimibe
NDC Package

Package Facts

Identity

Package NDC 82804-064-90
Digits Only 8280406490
Product NDC 82804-064
Description

90 TABLET in 1 BOTTLE (82804-064-90)

Marketing

Marketing Status
Marketed Since 2024-01-31
Brand ezetimibe
Generic ezetimibe
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "8b128e52-5d0d-4536-aa1f-be192d0989ad", "openfda": {"nui": ["N0000008553", "N0000175911"], "upc": ["0382804064304"], "unii": ["EOR26LQQ24"], "rxcui": ["349556"], "spl_set_id": ["8b128e52-5d0d-4536-aa1f-be192d0989ad"], "pharm_class_pe": ["Decreased Cholesterol Absorption [PE]"], "pharm_class_epc": ["Dietary Cholesterol Absorption Inhibitor [EPC]"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (82804-064-30)", "package_ndc": "82804-064-30", "marketing_start_date": "20240131"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (82804-064-60)", "package_ndc": "82804-064-60", "marketing_start_date": "20240131"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (82804-064-90)", "package_ndc": "82804-064-90", "marketing_start_date": "20240131"}], "brand_name": "Ezetimibe", "product_id": "82804-064_8b128e52-5d0d-4536-aa1f-be192d0989ad", "dosage_form": "TABLET", "pharm_class": ["Decreased Cholesterol Absorption [PE]", "Dietary Cholesterol Absorption Inhibitor [EPC]"], "product_ndc": "82804-064", "generic_name": "Ezetimibe", "labeler_name": "Proficient Rx LP", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ezetimibe", "active_ingredients": [{"name": "EZETIMIBE", "strength": "10 mg/1"}], "application_number": "ANDA209838", "marketing_category": "ANDA", "marketing_start_date": "20170825", "listing_expiration_date": "20261231"}