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"64764-720-07" National Drug Code (NDC)
Trintellix 1 BOTTLE in 1 CARTON (64764-720-07) / 7 TABLET, FILM COATED in 1 BOTTLE
(Takeda Pharmaceuticals America, Inc.)
NDC Code
64764-720-07
Package Description
1 BOTTLE in 1 CARTON (64764-720-07) / 7 TABLET, FILM COATED in 1 BOTTLE
Product NDC
64764-720
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Trintellix
Non-Proprietary Name
Vortioxetine
Dosage Form
TABLET, FILM COATED
Usage
ORAL
Start Marketing Date
20131002
Marketing Category Name
NDA
Application Number
NDA204447
Manufacturer
Takeda Pharmaceuticals America, Inc.
Substance Name
VORTIOXETINE HYDROBROMIDE
Strength
5
Strength Unit
mg/1
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/64764-720-07