GABAPENTIN
Summary
FDA approved GABAPENTIN by ZYDUS PHARMS USA INC. ANDA (Generic) approval (Labeling) on 2025-09-19. TABLET, ORAL.
Details
Source
Drug Approval
External ID
ANDA078926-20
Action Date
2025-09-19
Status
Approved
Category
drug
Product Code
ANDA (Generic)
Product Description
GABAPENTIN, TABLET, ORAL. Application: ANDA078926
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 "ANDA078926-20" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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