ALEVE LIQUID GELS (NAPROXEN SODIUM)
Summary
FDA approved ALEVE LIQUID GELS (NAPROXEN SODIUM) by PATHEON SOFTGELS. ANDA (Generic) approval (Labeling) on 2023-08-09. CAPSULE, ORAL.
Details
Source
Drug Approval
External ID
ANDA214463-1
Action Date
2023-08-09
Status
Approved
Category
drug
Product Code
ANDA (Generic)
Product Description
ALEVE LIQUID GELS (generic: NAPROXEN SODIUM), CAPSULE, ORAL. Application: ANDA214463
Company
Context & Analysis
Frequently Asked Questions
How often does PATHEON SOFTGELS have FDA actions?
This is the only FDA action we have on record for PATHEON SOFTGELS in our database.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "ANDA214463-1" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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