ezetimibe

Generic: ezetimibe

Labeler: bryant ranch prepack
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name ezetimibe
Generic Name ezetimibe
Labeler bryant ranch prepack
Dosage Form TABLET
Routes
ORAL
Active Ingredients

ezetimibe 10 mg/1

Manufacturer
Bryant Ranch Prepack

Identifiers & Regulatory

Product NDC 71335-2123
Product ID 71335-2123_34f7bf4b-9cfb-6931-e063-6394a90abab1
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA209838
Listing Expiration 2026-12-31
Marketing Start 2017-08-25

Pharmacologic Class

Established (EPC)
dietary cholesterol absorption inhibitor [epc]
Physiologic Effect
decreased cholesterol absorption [pe]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 713352123
Hyphenated Format 71335-2123

Supplemental Identifiers

RxCUI
349556
UNII
EOR26LQQ24
NUI
N0000008553 N0000175911

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 ANDA209838 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 10 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE (71335-2123-1)
  • 90 TABLET in 1 BOTTLE (71335-2123-2)
  • 28 TABLET in 1 BOTTLE (71335-2123-3)
  • 18 TABLET in 1 BOTTLE (71335-2123-4)
  • 60 TABLET in 1 BOTTLE (71335-2123-5)
source: ndc

Packages (5)

71335-2123-1 30 TABLET in 1 BOTTLE (71335-2123-1) 71335-2123-2 90 TABLET in 1 BOTTLE (71335-2123-2) 71335-2123-3 28 TABLET in 1 BOTTLE (71335-2123-3) 71335-2123-4 18 TABLET in 1 BOTTLE (71335-2123-4) 71335-2123-5 60 TABLET in 1 BOTTLE (71335-2123-5)

Ingredients (1)

ezetimibe (10 mg/1)

Linked Drug Pages (1)

Ezetimibe ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "34f7bf4b-9cfb-6931-e063-6394a90abab1", "openfda": {"nui": ["N0000008553", "N0000175911"], "unii": ["EOR26LQQ24"], "rxcui": ["349556"], "spl_set_id": ["3a80b668-51cd-42be-8497-8712b0508422"], "pharm_class_pe": ["Decreased Cholesterol Absorption [PE]"], "pharm_class_epc": ["Dietary Cholesterol Absorption Inhibitor [EPC]"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (71335-2123-1)", "package_ndc": "71335-2123-1", "marketing_start_date": "20220831"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (71335-2123-2)", "package_ndc": "71335-2123-2", "marketing_start_date": "20220824"}, {"sample": false, "description": "28 TABLET in 1 BOTTLE (71335-2123-3)", "package_ndc": "71335-2123-3", "marketing_start_date": "20240403"}, {"sample": false, "description": "18 TABLET in 1 BOTTLE (71335-2123-4)", "package_ndc": "71335-2123-4", "marketing_start_date": "20240403"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (71335-2123-5)", "package_ndc": "71335-2123-5", "marketing_start_date": "20231122"}], "brand_name": "Ezetimibe", "product_id": "71335-2123_34f7bf4b-9cfb-6931-e063-6394a90abab1", "dosage_form": "TABLET", "pharm_class": ["Decreased Cholesterol Absorption [PE]", "Dietary Cholesterol Absorption Inhibitor [EPC]"], "product_ndc": "71335-2123", "generic_name": "Ezetimibe", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ezetimibe", "active_ingredients": [{"name": "EZETIMIBE", "strength": "10 mg/1"}], "application_number": "ANDA209838", "marketing_category": "ANDA", "marketing_start_date": "20170825", "listing_expiration_date": "20261231"}