TOPIRAMATE
Summary
FDA approved TOPIRAMATE by ZYDUS PHARMS USA INC. ANDA (Generic) approval (Labeling) on 2023-09-08. CAPSULE, ORAL.
Details
Source
Drug Approval
External ID
ANDA078877-25
Action Date
2023-09-08
Status
Approved
Category
drug
Product Code
ANDA (Generic)
Product Description
TOPIRAMATE, CAPSULE, ORAL. Application: ANDA078877
Company
Context & Analysis
ZYDUS PHARMS USA INC has 7 FDA actions in our database.
Frequently Asked Questions
How often does ZYDUS PHARMS USA INC have FDA actions?
ZYDUS PHARMS USA INC has 7 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 "ANDA078877-25" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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