PREGABALIN EXTENDED RELEASE (PREGABALIN)
Summary
FDA approved PREGABALIN EXTENDED RELEASE (PREGABALIN) by SCIEGEN PHARMS. ANDA (Generic) approval on 2022-09-14. TABLET, EXTENDED RELEASE, ORAL.
Details
Source
Drug Approval
External ID
ANDA215675-1
Action Date
2022-09-14
Status
Approved
Category
drug
Product Code
ANDA (Generic)
Product Description
PREGABALIN EXTENDED RELEASE (generic: PREGABALIN), TABLET, EXTENDED RELEASE, ORAL. Application: ANDA215675
Company
Context & Analysis
SCIEGEN PHARMS has 20 FDA actions in our database.
Frequently Asked Questions
How often does SCIEGEN PHARMS have FDA actions?
SCIEGEN PHARMS has 20 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 "ANDA215675-1" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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