NABUMETONE
Summary
FDA approved NABUMETONE by IMPAX LABS INC. ANDA (Generic) approval (Labeling) on 2024-11-21. TABLET, ORAL.
Details
Source
Drug Approval
External ID
ANDA075189-32
Action Date
2024-11-21
Status
Approved
Category
drug
Product Code
ANDA (Generic)
Product Description
NABUMETONE, TABLET, ORAL. Application: ANDA075189
Company
Context & Analysis
IMPAX LABS INC has 11 FDA actions in our database.
Frequently Asked Questions
How often does IMPAX LABS INC have FDA actions?
IMPAX LABS INC has 11 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 "ANDA075189-32" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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