ezetimibe
Generic: ezetimibe
Labeler: a-s medication solutionsDrug Facts
Product Profile
Brand Name
ezetimibe
Generic Name
ezetimibe
Labeler
a-s medication solutions
Dosage Form
TABLET
Routes
Active Ingredients
ezetimibe 10 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
50090-7236
Product ID
50090-7236_6d15d418-3f41-4aca-aafb-a331a85df702
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA209234
Listing Expiration
2026-12-31
Marketing Start
2017-12-23
Pharmacologic Class
Established (EPC)
Physiologic Effect
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
500907236
Hyphenated Format
50090-7236
Supplemental Identifiers
RxCUI
UNII
NUI
Resolved Product View
Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.
Resolved Identity
Brand Name
ezetimibe (source: ndc)
Generic Name
ezetimibe (source: ndc)
Application Number
ANDA209234 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 10 mg/1
Packaging
- 90 TABLET in 1 BOTTLE (50090-7236-0)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "6d15d418-3f41-4aca-aafb-a331a85df702", "openfda": {"nui": ["N0000008553", "N0000175911"], "unii": ["EOR26LQQ24"], "rxcui": ["349556"], "spl_set_id": ["dd8a09cb-f014-4650-9da2-4ad1581c9741"], "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 (50090-7236-0)", "package_ndc": "50090-7236-0", "marketing_start_date": "20240828"}], "brand_name": "Ezetimibe", "product_id": "50090-7236_6d15d418-3f41-4aca-aafb-a331a85df702", "dosage_form": "TABLET", "pharm_class": ["Decreased Cholesterol Absorption [PE]", "Dietary Cholesterol Absorption Inhibitor [EPC]"], "product_ndc": "50090-7236", "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": "ANDA209234", "marketing_category": "ANDA", "marketing_start_date": "20171223", "listing_expiration_date": "20261231"}