This site is intended for healthcare professionals
Abstract digital waveforms in blue and purple
FDA Drug information

Ezetimibe

Read time: 1 mins
Marketing start date: 26 Nov 2024

Summary of product characteristics


Effective Time

20220826

Version

4

Spl Product Data Elements

ezetimibe ezetimibe EZETIMIBE EZETIMIBE CELLULOSE, MICROCRYSTALLINE CROSPOVIDONE LACTOSE MONOHYDRATE MAGNESIUM STEARATE POVIDONE SODIUM LAURYL SULFATE SODIUM STEARYL FUMARATE STARCH, CORN WHITE TO OFF-WHITE CAPSULE 773

Application Number

ANDA204331

Brand Name

Ezetimibe

Generic Name

ezetimibe

Product Ndc

70771-1109

Product Type

HUMAN PRESCRIPTION DRUG

Route

ORAL

Package Label Principal Display Panel

NDC 70771-1109-3 in bottle of 30 tablets Ezetimibe Tablets , 10 mg Rx only 30 tablets Ezetimibe Tablets, 10 mg

Learning Zones

The Learning Zones are an educational resource for healthcare professionals that provide medical information on the epidemiology, pathophysiology and burden of disease, as well as diagnostic techniques and treatment regimens.

Disclaimer

The drug Prescribing Information (PI), including indications, contra-indications, interactions, etc, has been developed using the U.S. Food & Drug Administration (FDA) as a source (www.fda.gov).

Medthority offers the whole library of PI documents from the FDA. Medthority will not be held liable for explicit or implicit errors, or missing data.

Drugs appearing in this section are approved by the FDA. For regions outside of the United States, this content is for informational purposes only and may not be aligned with local regulatory approvals or guidance.