NAPROXEN SODIUM
Summary
FDA approved NAPROXEN SODIUM by HETERO LABS LTD V. ANDA (Generic) approval on 2022-10-28. TABLET, ORAL.
Details
Source
Drug Approval
External ID
ANDA211065-1
Action Date
2022-10-28
Status
Approved
Category
drug
Product Code
ANDA (Generic)
Product Description
NAPROXEN SODIUM, TABLET, ORAL. Application: ANDA211065
Company
Context & Analysis
HETERO LABS LTD V has 27 FDA actions in our database.
Frequently Asked Questions
How often does HETERO LABS LTD V have FDA actions?
HETERO LABS LTD V has 27 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 "ANDA211065-1" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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