Medical emergency?Emergency? Call 911. Nearest emergency roomsNearest ERs

Drug company (FDA labeler)

Vertex Pharmaceuticals Incorporated

NDC labeler code: 51167

What is a labeler?

The company whose name is on the package and in the FDA’s National Drug Code (NDC) Directory. It may make the medicine itself or sell medicine made by another company. The first part of every NDC code identifies the labeler.

Official FDA data only

Products, approvals and recalls come from the FDA (NDC Directory, Drugs@FDA, enforcement reports). Recalls are linked to this company by the NDC labeler code on the recalled product.

Questions about your medicine: ask your doctor or pharmacist. In an emergency, call 911.

At a glance

14Products (NDC)

Prescription medicines

FDA applications for these products

  • NDA: New Drug Application: how a new (usually brand-name) medicine is approved.
ApprovedApplicationMedicineSponsor
January 30, 2025NDA219209 Suzetrigine
JOURNAVX
Vertex Pharms Inc
December 20, 2024NDA218730 Vanzacaftor, tezacaftor, and deutivacaftor
ALYFTREK
Vertex Pharms Inc
August 7, 2018NDA211358 Lumacaftor and ivacaftor
ORKAMBI
Vertex Pharms Inc
July 2, 2015NDA206038 Lumacaftor and ivacaftor
ORKAMBI
Vertex Pharms Inc
March 17, 2015NDA207925 Ivacaftor
KALYDECO
Vertex Pharms Inc
January 31, 2012NDA203188 Ivacaftor
KALYDECO
Vertex Pharms

The sponsor is the company that holds the FDA application; it can differ from the labeler.

Recall timeline

No recall of these products (by NDC code) appears in the FDA enforcement reports.

Sources

  1. NDC Directory (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 30, 2026, retrieved October 31, 2026
  2. Drugs@FDA (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 30, 2026, retrieved October 31, 2026
  3. Drug recall enforcement reports (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 27, 2026, retrieved October 31, 2026

FDA Enforcement Report search → · Report an error →