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"0615-7565-39" National Drug Code (NDC)
Topiramate 30 TABLET, FILM COATED in 1 BLISTER PACK (0615-7565-39)
(NCS HealthCare of KY, Inc dba Vangard Labs)
NDC Code
0615-7565-39
Package Description
30 TABLET, FILM COATED in 1 BLISTER PACK (0615-7565-39)
Product NDC
0615-7565
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Topiramate
Non-Proprietary Name
Topiramate
Dosage Form
TABLET, FILM COATED
Usage
ORAL
Start Marketing Date
20090327
Marketing Category Name
ANDA
Application Number
ANDA078235
Manufacturer
NCS HealthCare of KY, Inc dba Vangard Labs
Substance Name
TOPIRAMATE
Strength
200
Strength Unit
mg/1
Pharmacy Classes
Decreased Central Nervous System Disorganized Electrical Activity [PE],Cytochrome P450 3A4 Inducers [MoA],Cytochrome P450 2C19 Inhibitors [MoA]
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/0615-7565-39