Package 68382-773-05
Brand: ezetimibe
Generic: ezetimibePackage Facts
Identity
Package NDC
68382-773-05
Digits Only
6838277305
Product NDC
68382-773
Description
500 TABLET in 1 BOTTLE (68382-773-05)
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": "ebb60f24-14be-4be0-b5e2-31e695eae876", "openfda": {"nui": ["N0000008553", "N0000175911"], "unii": ["EOR26LQQ24"], "rxcui": ["349556"], "spl_set_id": ["f852b12f-e25f-415b-b1e2-58955d609507"], "pharm_class_pe": ["Decreased Cholesterol Absorption [PE]"], "pharm_class_epc": ["Dietary Cholesterol Absorption Inhibitor [EPC]"], "manufacturer_name": ["Zydus Pharmaceuticals USA Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (68382-773-01)", "package_ndc": "68382-773-01", "marketing_start_date": "20170809"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (68382-773-05)", "package_ndc": "68382-773-05", "marketing_start_date": "20170809"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (68382-773-06)", "package_ndc": "68382-773-06", "marketing_start_date": "20170809"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (68382-773-10)", "package_ndc": "68382-773-10", "marketing_start_date": "20170809"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (68382-773-16)", "package_ndc": "68382-773-16", "marketing_start_date": "20170809"}, {"sample": false, "description": "10 BLISTER PACK in 1 CARTON (68382-773-77) / 10 TABLET in 1 BLISTER PACK (68382-773-30)", "package_ndc": "68382-773-77", "marketing_start_date": "20170809"}], "brand_name": "ezetimibe", "product_id": "68382-773_ebb60f24-14be-4be0-b5e2-31e695eae876", "dosage_form": "TABLET", "pharm_class": ["Decreased Cholesterol Absorption [PE]", "Dietary Cholesterol Absorption Inhibitor [EPC]"], "product_ndc": "68382-773", "generic_name": "ezetimibe", "labeler_name": "Zydus Pharmaceuticals USA Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "ezetimibe", "active_ingredients": [{"name": "EZETIMIBE", "strength": "10 mg/1"}], "application_number": "ANDA204331", "marketing_category": "ANDA", "marketing_start_date": "20170809", "listing_expiration_date": "20261231"}