OLMESARTAN MEDOXOMIL
Summary
FDA approved OLMESARTAN MEDOXOMIL by ZYDUS PHARMS. ANDA (Generic) approval (Labeling) on 2022-07-01. TABLET, ORAL.
Details
Source
Drug Approval
External ID
ANDA205192-1
Action Date
2022-07-01
Status
Approved
Category
drug
Product Code
ANDA (Generic)
Product Description
OLMESARTAN MEDOXOMIL, TABLET, ORAL. Application: ANDA205192
Company
Context & Analysis
ZYDUS PHARMS has 60 FDA actions in our database.
Frequently Asked Questions
How often does ZYDUS PHARMS have FDA actions?
ZYDUS PHARMS has 60 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 "ANDA205192-1" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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