Package 0781-5690-92

Brand: ezetimibe

Generic: ezetimibe
NDC Package

Package Facts

Identity

Package NDC 0781-5690-92
Digits Only 0781569092
Product NDC 0781-5690
Description

90 TABLET in 1 BOTTLE (0781-5690-92)

Marketing

Marketing Status
Marketed Since 2017-06-12
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": "c5e4a665-e54b-4452-bbc7-0a75b633ea94", "openfda": {"nui": ["N0000008553", "N0000175911"], "unii": ["EOR26LQQ24"], "rxcui": ["349556"], "spl_set_id": ["ebcb6655-fd60-4099-8099-be911c5b32ae"], "pharm_class_pe": ["Decreased Cholesterol Absorption [PE]"], "pharm_class_epc": ["Dietary Cholesterol Absorption Inhibitor [EPC]"], "manufacturer_name": ["Sandoz Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "500 TABLET in 1 BOTTLE (0781-5690-05)", "package_ndc": "0781-5690-05", "marketing_start_date": "20170612"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (0781-5690-31)", "package_ndc": "0781-5690-31", "marketing_start_date": "20170612"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (0781-5690-92)", "package_ndc": "0781-5690-92", "marketing_start_date": "20170612"}], "brand_name": "Ezetimibe", "product_id": "0781-5690_c5e4a665-e54b-4452-bbc7-0a75b633ea94", "dosage_form": "TABLET", "pharm_class": ["Decreased Cholesterol Absorption [PE]", "Dietary Cholesterol Absorption Inhibitor [EPC]"], "product_ndc": "0781-5690", "generic_name": "Ezetimibe", "labeler_name": "Sandoz Inc", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ezetimibe", "active_ingredients": [{"name": "EZETIMIBE", "strength": "10 mg/1"}], "application_number": "ANDA203931", "marketing_category": "ANDA", "marketing_start_date": "20170612", "listing_expiration_date": "20261231"}