United States · FDA National Drug Code directory

ORKAMBI

A source-listed medicine record.

Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.

Medicine identity

Source reference
51167-809_e746b83a-cec1-40ab-8dba-7d8c1781e8b1
Product NDC
51167-809
Form
TABLET, FILM COATED
Composition / generic term
lumacaftor and ivacaftor
Labeler
Vertex Pharmaceuticals Incorporated
Marketing category
NDA
Marketing start / end (source format)
20150702
Source listing expiry
20271231

Source-listed ingredients

  • LUMACAFTOR — 200 mg/1
  • IVACAFTOR — 125 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 4 CARTON in 1 BOX (51167-809-01) / 7 BLISTER PACK in 1 CARTON / 4 TABLET, FILM COATED in 1 BLISTER PACK · 51167-809-01

Source and coverage

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Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.

Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.

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