ezetimibe

Generic: ezetimibe

Labeler: proficient rx lp
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name ezetimibe
Generic Name ezetimibe
Labeler proficient rx lp
Dosage Form TABLET
Routes
ORAL
Active Ingredients

ezetimibe 10 mg/1

Manufacturer
Proficient Rx LP

Identifiers & Regulatory

Product NDC 71205-277
Product ID 71205-277_4f9db4e9-1b45-4c0e-ae3c-068627f5a953
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)
dietary cholesterol absorption inhibitor [epc]
Physiologic Effect
decreased cholesterol absorption [pe]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 71205277
Hyphenated Format 71205-277

Supplemental Identifiers

RxCUI
349556
UPC
0371205277307
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 ANDA209234 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 10 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE (71205-277-30)
  • 60 TABLET in 1 BOTTLE (71205-277-60)
  • 90 TABLET in 1 BOTTLE (71205-277-90)
source: ndc

Packages (3)

71205-277-30 30 TABLET in 1 BOTTLE (71205-277-30) 71205-277-60 60 TABLET in 1 BOTTLE (71205-277-60) 71205-277-90 90 TABLET in 1 BOTTLE (71205-277-90)

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": "4f9db4e9-1b45-4c0e-ae3c-068627f5a953", "openfda": {"nui": ["N0000008553", "N0000175911"], "upc": ["0371205277307"], "unii": ["EOR26LQQ24"], "rxcui": ["349556"], "spl_set_id": ["fbbe54c3-59a1-436c-aba8-188ba7ca70e0"], "pharm_class_pe": ["Decreased Cholesterol Absorption [PE]"], "pharm_class_epc": ["Dietary Cholesterol Absorption Inhibitor [EPC]"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (71205-277-30)", "package_ndc": "71205-277-30", "marketing_start_date": "20190501"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (71205-277-60)", "package_ndc": "71205-277-60", "marketing_start_date": "20190501"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (71205-277-90)", "package_ndc": "71205-277-90", "marketing_start_date": "20190501"}], "brand_name": "Ezetimibe", "product_id": "71205-277_4f9db4e9-1b45-4c0e-ae3c-068627f5a953", "dosage_form": "TABLET", "pharm_class": ["Decreased Cholesterol Absorption [PE]", "Dietary Cholesterol Absorption Inhibitor [EPC]"], "product_ndc": "71205-277", "generic_name": "Ezetimibe", "labeler_name": "Proficient Rx LP", "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"}