Package 51660-200-30
Brand: ezetimibe
Generic: ezetimibePackage Facts
Identity
Package NDC
51660-200-30
Digits Only
5166020030
Product NDC
51660-200
Description
30 TABLET in 1 BOTTLE (51660-200-30)
Marketing
Marketing Status
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": "12e7e79e-85d0-0c5d-e063-6394a90a8b78", "openfda": {"nui": ["N0000008553", "N0000175911"], "upc": ["0351660200300", "0351660200904"], "unii": ["EOR26LQQ24"], "rxcui": ["349556"], "spl_set_id": ["5b3842f6-c80a-47b8-8a82-b69e465b05f7"], "pharm_class_pe": ["Decreased Cholesterol Absorption [PE]"], "pharm_class_epc": ["Dietary Cholesterol Absorption Inhibitor [EPC]"], "manufacturer_name": ["Ohm Laboratories Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "500 TABLET in 1 BOTTLE (51660-200-05)", "package_ndc": "51660-200-05", "marketing_start_date": "20170612"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (51660-200-30)", "package_ndc": "51660-200-30", "marketing_start_date": "20170612"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (51660-200-90)", "package_ndc": "51660-200-90", "marketing_start_date": "20170612"}], "brand_name": "Ezetimibe", "product_id": "51660-200_12e7e79e-85d0-0c5d-e063-6394a90a8b78", "dosage_form": "TABLET", "pharm_class": ["Decreased Cholesterol Absorption [PE]", "Dietary Cholesterol Absorption Inhibitor [EPC]"], "product_ndc": "51660-200", "generic_name": "Ezetimibe", "labeler_name": "Ohm Laboratories Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ezetimibe", "active_ingredients": [{"name": "EZETIMIBE", "strength": "10 mg/1"}], "application_number": "ANDA207311", "marketing_category": "ANDA", "marketing_start_date": "20170612", "listing_expiration_date": "20261231"}