ESCITALOPRAM OXALATE
Summary
FDA approved ESCITALOPRAM OXALATE by ZYDUS LIFESCIENCES. ANDA (Generic) approval (Labeling) on 2025-06-06. TABLET, ORAL.
Details
Source
Drug Approval
External ID
ANDA077734-3
Action Date
2025-06-06
Status
Approved
Category
drug
Product Code
ANDA (Generic)
Product Description
ESCITALOPRAM OXALATE, TABLET, ORAL. Application: ANDA077734
Company
Context & Analysis
ZYDUS LIFESCIENCES has 37 FDA actions in our database.
Frequently Asked Questions
How often does ZYDUS LIFESCIENCES have FDA actions?
ZYDUS LIFESCIENCES has 37 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 "ANDA077734-3" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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