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"64764-580-07" National Drug Code (NDC)

Brintellix 1 BOTTLE in 1 CARTON (64764-580-07) > 7 TABLET, FILM COATED in 1 BOTTLE
(Takeda Pharmaceuticals America, Inc.)

NDC Code64764-580-07
Package Description1 BOTTLE in 1 CARTON (64764-580-07) > 7 TABLET, FILM COATED in 1 BOTTLE
Product NDC64764-580
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameBrintellix
Non-Proprietary NameVortioxetine
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20131002
Marketing Category NameNDA
Application NumberNDA204447
ManufacturerTakeda Pharmaceuticals America, Inc.
Substance NameVORTIOXETINE HYDROBROMIDE
Strength20
Strength Unitmg/1

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/64764-580-07





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