Package 50090-7689-0

Brand: ezetimibe

Generic: ezetimibe
NDC Package

Package Facts

Identity

Package NDC 50090-7689-0
Digits Only 5009076890
Product NDC 50090-7689
Description

90 TABLET in 1 BOTTLE (50090-7689-0)

Marketing

Marketing Status
Marketed Since 2025-10-10
Brand ezetimibe
Generic ezetimibe
Sample Package No

Linked Drug Pages (0)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "fbc0bed9-2a61-4400-867d-442488449348", "openfda": {"nui": ["N0000008553", "N0000175911"], "unii": ["EOR26LQQ24"], "rxcui": ["349556"], "spl_set_id": ["4158aa71-3540-4912-b909-7491e5a1429c"], "pharm_class_pe": ["Decreased Cholesterol Absorption [PE]"], "pharm_class_epc": ["Dietary Cholesterol Absorption Inhibitor [EPC]"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE (50090-7689-0)", "package_ndc": "50090-7689-0", "marketing_start_date": "20251010"}], "brand_name": "EZETIMIBE", "product_id": "50090-7689_fbc0bed9-2a61-4400-867d-442488449348", "dosage_form": "TABLET", "pharm_class": ["Decreased Cholesterol Absorption [PE]", "Dietary Cholesterol Absorption Inhibitor [EPC]"], "product_ndc": "50090-7689", "generic_name": "EZETIMIBE", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "EZETIMIBE", "active_ingredients": [{"name": "EZETIMIBE", "strength": "10 mg/1"}], "application_number": "ANDA210859", "marketing_category": "ANDA", "marketing_start_date": "20220726", "listing_expiration_date": "20261231"}