"51167-331-01" National Drug Code (NDC)

Trikafta 4 BLISTER PACK in 1 CARTON (51167-331-01) / 1 KIT in 1 BLISTER PACK * 14 TABLET, FILM COATED in 1 BLISTER PACK (51167-431-14) * 7 TABLET, FILM COATED in 1 BLISTER PACK (51167-531-07)
(Vertex Pharmaceuticals Incorporated)

NDC Code51167-331-01
Package Description4 BLISTER PACK in 1 CARTON (51167-331-01) / 1 KIT in 1 BLISTER PACK * 14 TABLET, FILM COATED in 1 BLISTER PACK (51167-431-14) * 7 TABLET, FILM COATED in 1 BLISTER PACK (51167-531-07)
Product NDC51167-331
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameTrikafta
Non-Proprietary NameElexacaftor, Tezacaftor, And Ivacaftor
Dosage FormKIT
Start Marketing Date20191021
Marketing Category NameNDA
Application NumberNDA212273
ManufacturerVertex Pharmaceuticals Incorporated

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