"55154-0257-8" National Drug Code (NDC)

Trintellix 2430 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (55154-0257-8)
(Cardinal Health 107, LLC)

NDC Code55154-0257-8
Package Description2430 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (55154-0257-8)
Product NDC55154-0257
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameTrintellix
Non-Proprietary NameVortioxetine
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20131002
Marketing Category NameNDA
Application NumberNDA204447
ManufacturerCardinal Health 107, LLC
Substance NameVORTIOXETINE HYDROBROMIDE
Strength20
Strength Unitmg/1

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