Orkambi - Lumacaftor and ivacaftor 125 mg / 1; 200 mg / 1 Tablet 4 Carton

Reference details for licensed healthcare facility review and verification.

lumacaftor and ivacaftor NDC Family 51167-0809 lumacaftor and ivacaftor 125 mg / 1; 200 mg / 1

NDC 11	51167-0809-01
Product NDC	51167-0809
Generic Drug Name	lumacaftor and ivacaftor
Brand Name	Orkambi
Manufacturer	Vertex Pharmaceuticals Incorporated
Strength	125 mg / 1; 200 mg / 1
Dosage Form	Tablet
Drug Type	Oral
Package Quantity	4 Carton
Package Description	4 CARTON in 1 BOX (51167-809-01) / 7 BLISTER PACK in 1 CARTON / 4 TABLET, FILM COATED in 1 BLISTER PACK
Active Ingredients	Ivacaftor; Lumacaftor
Marketing Category	NDA

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NDC snapshot

lumacaftor and ivacaftor 125 mg / 1; 200 mg / 1 Tablet is tracked under NDC 51167-0809-01 and rolls up into product family 51167-0809. Use this page to confirm the exact presentation before comparing related family pages or starting a quote review.

Package configuration: 4 Carton.
Manufacturer: Vertex Pharmaceuticals Incorporated.
Dosage form: Tablet.
Family size: 1 indexed presentation.

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Official references

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Orkambi - Lumacaftor and ivacaftor 125 mg / 1; 200 mg / 1 Tablet 4 Carton, NDC 51167-0809-01, is a Vertex Pharmaceuticals Incorporated 125 mg / 1; 200 mg / 1 tablet presentation packaged as 4 Carton.

NDC search formats

Canonical NDC 11: 51167-0809-01
Digits-only NDC 11: 51167080901
Possible 10-digit display formats: 51167-809-01 (5116780901), 51167-0809-1 (5116708091)

Multiple 10-digit display-format aliases can map to the same stored 11-digit billing NDC, so these are shown as search aliases rather than a single asserted package format.

Helpful product links

Search by brand name: Orkambi
Exact NDC 11: 51167-0809-01
Product family NDC: 51167-0809
VA classification code: RE900
VA classification code description: RESPIRATORY AGENTS,OTHER
CMOP ID: I0601
VUID: 4034619