NDC 51167-809 – Orkambi
Lumacaftor 200 mg/1; Ivacaftor 125 mg/1 · Tablet, Film Coated · Oral
Product NDC51167-809
Product details
- Brand name
- Orkambi
- Generic name
- Lumacaftor and ivacaftor
- Labeler
- Vertex Pharmaceuticals Incorporated
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- NDA · NDA206038
- Marketed since
- July 2, 2015
- Listing expires
- December 31, 2027
- Pharmacologic class
- Cystic Fibrosis Transmembrane Conductance Regulator Potentiator
Active ingredients
- Lumacaftor 200 mg/1
- Ivacaftor 125 mg/1
Package NDC codes (1)
| Package NDC | Description | Since |
|---|---|---|
| 51167-809-01 | 4 CARTON in 1 BOX (51167-809-01) / 7 BLISTER PACK in 1 CARTON / 4 TABLET, FILM COATED in 1 BLISTER PACK | Jul 2, 2015 |
Other Orkambi products
- 51167-700 Lumacaftor 100 mg/1; Ivacaftor 125 mg/1 · Tablet, Film Coated · Vertex Pharmaceuticals Incorporated
- 51167-122 Lumacaftor 75 mg/1; Ivacaftor 94 mg/1 · Granule · Vertex Pharmaceuticals Incorporated
- 51167-500 Lumacaftor 150 mg/1; Ivacaftor 188 mg/1 · Granule · Vertex Pharmaceuticals Incorporated
- 51167-900 Lumacaftor 100 mg/1; Ivacaftor 125 mg/1 · Granule · Vertex Pharmaceuticals Incorporated