Source facts
FDA issued an approval letter for FOCINVEZ on 2026-03-31. The source metadata identifies NDA 216686 as a supplement. Review the exact FDA letter for the approved conditions and labeling.
US FDA source recordAL · Approval Letter
FOCINVEZ — FDA Approval Letter (NDA 216686)
Issued to STERISCIENCE. Application is approved as submitted.
Issued
March 31, 2026Application
NDA 505b1 • 216686
Product
FOCINVEZ
Company
STERISCIENCE
Stage
Final Decision
Assyro regulatory brief
FreeWhat did FDA decide for FOCINVEZ?
Source facts and Assyro context are separated so you can scan the action quickly without treating analysis as an FDA conclusion.
Key details in this letter
- 1FDA action: approval.
- 2Application: NDA 216686.
- 3Submission: supplement.
- 4Sponsor: STERISCIENCE.
Suggested next step
Review the exact FDA letter for approved conditions, labeling, and postmarketing requirements.
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Common questions about the FOCINVEZ approval letter
Is FOCINVEZ FDA approved?
This letter documents an FDA approval action: FDA approved NDA 216686 for FOCINVEZ, sponsored by STERISCIENCE, on March 31, 2026. Product may be marketed. Verify current status and labeling in the source letter, since later FDA actions can change them.
What is NDA 216686?
NDA 216686 is the application under which FDA issued this approval letter for FOCINVEZ to STERISCIENCE. The letter is dated March 31, 2026.
What happens after an FDA approval letter?
The sponsor may market the product in line with the approved labeling. Approval letters typically set post-approval obligations: submitting final content of labeling, meeting any postmarketing requirements or commitments listed in the letter, updating Orange Book patent information within 30 days for NDAs, and ongoing annual reporting under 21 CFR 314.81.