ESCITALOPRAM OXALATE
Summary
FDA approved ESCITALOPRAM OXALATE by HETERO LABS LTD III. ANDA (Generic) approval (Labeling) on 2024-05-30. SOLUTION, ORAL.
Details
Source
Drug Approval
External ID
ANDA202221-15
Action Date
2024-05-30
Status
Approved
Category
drug
Product Code
ANDA (Generic)
Product Description
ESCITALOPRAM OXALATE, SOLUTION, ORAL. Application: ANDA202221
Company
Context & Analysis
HETERO LABS LTD III has 21 FDA actions in our database.
Frequently Asked Questions
How often does HETERO LABS LTD III have FDA actions?
HETERO LABS LTD III has 21 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 "ANDA202221-15" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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