NABUMETONE
Summary
FDA approved NABUMETONE by AUROBINDO PHARMA USA. ANDA (Generic) approval (Labeling) on 2024-11-21. TABLET, ORAL.
Details
Source
Drug Approval
External ID
ANDA090516-5
Action Date
2024-11-21
Status
Approved
Category
drug
Product Code
ANDA (Generic)
Product Description
NABUMETONE, TABLET, ORAL. Application: ANDA090516
Company
Context & Analysis
AUROBINDO PHARMA USA has 8 FDA actions in our database.
Frequently Asked Questions
How often does AUROBINDO PHARMA USA have FDA actions?
AUROBINDO PHARMA USA has 8 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 "ANDA090516-5" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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