NAPROXEN AND ESOMEPRAZOLE MAGNESIUM
Summary
FDA approved NAPROXEN AND ESOMEPRAZOLE MAGNESIUM by SCIEGEN PHARMS. ANDA (Generic) approval (Labeling) on 2024-11-21. TABLET, DELAYED RELEASE, ORAL.
Details
Source
Drug Approval
External ID
ANDA217738-1
Action Date
2024-11-21
Status
Approved
Category
drug
Product Code
ANDA (Generic)
Product Description
NAPROXEN AND ESOMEPRAZOLE MAGNESIUM, TABLET, DELAYED RELEASE, ORAL. Application: ANDA217738
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 "ANDA217738-1" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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