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US FDA source recordAL · Approval Letter

HYRNUO — FDA Approval Letter (NDA 219972)

Issued to BAYER HEALTHCARE. Application is approved as submitted.

Posted by FDA

September 10, 2026

Application

NDA 505b1 • 219972

Product

HYRNUO

Company

BAYER HEALTHCARE

Stage

Final Decision

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What did FDA decide for HYRNUO?

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Verify in source

Source facts

FDA posted an approval letter for HYRNUO on 2026-09-10. This is the document posting date; consult the signed letter for the decision date. The source metadata identifies NDA 219972 as a supplement. Review the exact FDA letter for the approved conditions and labeling.

Key details in this letter

  • 1FDA action: approval.
  • 2Application: NDA 219972.
  • 3Submission: supplement.
  • 4Sponsor: BAYER HEALTHCARE.

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 HYRNUO approval letter

Is HYRNUO FDA approved?

This letter documents an FDA approval action: FDA approved NDA 219972 for HYRNUO, sponsored by BAYER HEALTHCARE,. Product may be marketed. Verify current status and labeling in the source letter, since later FDA actions can change them.

What is NDA 219972?

NDA 219972 is the application under which FDA issued this approval letter for HYRNUO to BAYER HEALTHCARE. FDA posted the letter on September 10, 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.