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
50090-7689
Product ID
50090-7689_fbc0bed9-2a61-4400-867d-442488449348
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA210859
Listing Expiration
2026-12-31
Marketing Start
2022-07-26
Pharmacologic Class
Established (EPC)
Physiologic Effect
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
500907689
Hyphenated Format
50090-7689
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
ANDA210859 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 10 mg/1
Packaging
- 90 TABLET in 1 BOTTLE (50090-7689-0)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
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"}