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US FDA source recordAL · Approval Letter

PIFELTRO — FDA Approval Letter (NDA 210806)

Issued to MSD MERCK CO. Application is approved as submitted.

Posted by FDA

October 1, 2026

Application

NDA 505b1 • 210806

Product

PIFELTRO

Company

MSD MERCK CO

Stage

Final Decision

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What did FDA decide for PIFELTRO?

Source facts and Assyro context are separated so you can scan the action quickly without treating analysis as an FDA conclusion.

Verify in source

Source facts

FDA posted an approval letter for PIFELTRO on 2026-10-01. This is the document posting date; consult the signed letter for the decision date. The source metadata identifies NDA 210806 as a supplement. Review the exact FDA letter for the approved conditions and labeling.

Key details in this letter

  • 1FDA action: approval.
  • 2Application: NDA 210806.
  • 3Submission: supplement.
  • 4Sponsor: MSD MERCK CO.

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

Read the full FDA approval letter (PDF)

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Common questions about the PIFELTRO approval letter

Is PIFELTRO FDA approved?

This letter documents an FDA approval action: FDA approved NDA 210806 for PIFELTRO, sponsored by MSD MERCK CO,. Product may be marketed. Verify current status and labeling in the source letter, since later FDA actions can change them.

What is NDA 210806?

NDA 210806 is the application under which FDA issued this approval letter for PIFELTRO to MSD MERCK CO. FDA posted the letter on October 1, 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.