"64764-730-09" National Drug Code (NDC)

Trintellix 30 TABLET, FILM COATED in 1 BOTTLE (64764-730-09)
(Takeda Pharmaceuticals America, Inc.)

NDC Code64764-730-09
Package Description30 TABLET, FILM COATED in 1 BOTTLE (64764-730-09)
Product NDC64764-730
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameTrintellix
Non-Proprietary NameVortioxetine
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20131002
Marketing Category NameNDA
Application NumberNDA204447
ManufacturerTakeda Pharmaceuticals America, Inc.
Substance NameVORTIOXETINE HYDROBROMIDE
Strength10
Strength Unitmg/1

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