# ORKAMBI

NDC: 51167-900
Generic name: lumacaftor and ivacaftor
Labeler / Manufacturer: Vertex Pharmaceuticals Incorporated
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: New Drug Application (innovator)
Dosage form: GRANULE
Routes: ORAL
Marketing started: 20180807

FDA application: NDA211358

## Active ingredients

- IVACAFTOR: 125 mg/1
- LUMACAFTOR: 100 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"51167-900"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=51167-900
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=3fc1c40e-cfac-47a1-9e1a-61ead3570600