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US FDA source recordAL · Approval Letter

ZIIHERA — FDA Approval Letter (BLA 761416)

Issued to JAZZ PHARMS. Application is approved as submitted.

Posted by FDA

August 27, 2026

Application

BLA • 761416

Product

ZIIHERA

Company

JAZZ PHARMS

Stage

Final Decision

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What did FDA decide for ZIIHERA?

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Verify in source

Source facts

FDA posted an approval letter for ZIIHERA on 2026-08-27. This is the document posting date; consult the signed letter for the decision date. The source metadata identifies BLA 761416 as a supplement. Review the exact FDA letter for the approved conditions and labeling.

Key details in this letter

  • 1FDA action: approval.
  • 2Application: BLA 761416.
  • 3Submission: supplement.
  • 4Sponsor: JAZZ PHARMS.

Suggested next step

Review the exact FDA letter for approved conditions, labeling, and postmarketing requirements.

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Built from structured FDA metadata and deterministic source-text signals. Topic matches are navigation aids, not legal or regulatory conclusions. Verify material decisions against the original FDA document.

FDAPDFUpdated Oct 8, 2026

FDA source document

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Common questions about the ZIIHERA approval letter

Is ZIIHERA FDA approved?

This letter documents an FDA approval action: FDA approved BLA 761416 for ZIIHERA, sponsored by JAZZ PHARMS,. Product may be marketed. Verify current status and labeling in the source letter, since later FDA actions can change them.

What is BLA 761416?

BLA 761416 is the application under which FDA issued this approval letter for ZIIHERA to JAZZ PHARMS. FDA posted the letter on August 27, 2026; the posting date is not the decision date.

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.