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"0051-0630-08" National Drug Code (NDC)
Vortioxetine 1 BOTTLE in 1 CARTON (0051-0630-08) > 7 TABLET, FILM COATED in 1 BOTTLE
(AbbVie Inc.)
NDC Code
0051-0630-08
Package Description
1 BOTTLE in 1 CARTON (0051-0630-08) > 7 TABLET, FILM COATED in 1 BOTTLE
Product NDC
0051-0630
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Vortioxetine
Non-Proprietary Name
Vortioxetine
Dosage Form
TABLET, FILM COATED
Usage
ORAL
Start Marketing Date
20131002
End Marketing Date
20200531
Marketing Category Name
APPROVED DRUG PRODUCT MANUFACTURED UNDER CONTRACT
Application Number
NDA204447
Manufacturer
AbbVie Inc.
Substance Name
VORTIOXETINE HYDROBROMIDE
Strength
5
Strength Unit
mg/1
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/0051-0630-08