Source facts
FDA issued a tentative approval letter for CEFTRIAXONE on 2026-07-21. The source metadata identifies ANDA 210197 as an original application. Review the exact FDA letter for the approved conditions and labeling.
US FDA source recordTA · Tentative Approval Letter
CEFTRIAXONE — FDA Tentative Approval Letter (ANDA 210197)
Issued to DEVA HOLDING AS. Application meets requirements but marketing is blocked (patent/exclusivity).
Issued
July 21, 2026Application
ANDA 505j • 210197
Product
CEFTRIAXONE
Company
DEVA HOLDING AS
Stage
Final Decision
Assyro regulatory brief
FreeWhat did FDA decide for CEFTRIAXONE?
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: tentative approval.
- 2Application: ANDA 210197.
- 3Submission: original application.
- 4Sponsor: DEVA HOLDING AS.
Suggested next step
Review the exact FDA letter for approved conditions, labeling, and postmarketing requirements.
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Common questions about the CEFTRIAXONE tentative approval letter
Is CEFTRIAXONE FDA approved?
Not for marketing yet. FDA granted tentative approval to ANDA 210197 for CEFTRIAXONE on July 21, 2026, meaning the application meets approval standards but patent or exclusivity protections block final approval. The product cannot be marketed until those conditions resolve and FDA issues final approval.
What is ANDA 210197?
ANDA 210197 is the application under which FDA issued this tentative approval letter for CEFTRIAXONE to DEVA HOLDING AS. The letter is dated July 21, 2026.
What happens after an FDA tentative approval letter?
The product cannot be marketed yet. Tentative approval means the application meets FDA approval standards, but patent or exclusivity protections block final approval. The sponsor typically requests final approval as the blocking date approaches, and FDA re-verifies that the approval conditions still hold before granting it.