OXYCODONE AND ACETAMINOPHEN
Summary
FDA approved OXYCODONE AND ACETAMINOPHEN by SANALUZ. ANDA (Generic) approval (REMS) on 2026-06-18. TABLET, ORAL.
Details
Source
Drug Approval
External ID
ANDA207574-14
Action Date
2026-06-18
Status
Approved
Category
drug
Product Code
ANDA (Generic)
Product Description
OXYCODONE AND ACETAMINOPHEN, TABLET, ORAL. Application: ANDA207574
Company
Context & Analysis
Frequently Asked Questions
How often does SANALUZ have FDA actions?
This is the only FDA action we have on record for SANALUZ in our database.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "ANDA207574-14" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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