EZETIMIBE
Summary
FDA approved EZETIMIBE by GLENMARK PHARMS LTD. ANDA (Generic) approval (Labeling) on 2024-06-03. TABLET, ORAL.
Details
Source
Drug Approval
External ID
ANDA078560-11
Action Date
2024-06-03
Status
Approved
Category
drug
Product Code
ANDA (Generic)
Product Description
EZETIMIBE, TABLET, ORAL. Application: ANDA078560
Company
Context & Analysis
GLENMARK PHARMS LTD has 36 FDA actions in our database.
Frequently Asked Questions
How often does GLENMARK PHARMS LTD have FDA actions?
GLENMARK PHARMS LTD has 36 FDA actions in our database, including 0 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "ANDA078560-11" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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