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"58118-0712-0" National Drug Code (NDC)
Topiramate 1 TABLET, FILM COATED in 1 PACKET (58118-0712-0)
(Clinical Solutions Wholesale)
NDC Code
58118-0712-0
Package Description
1 TABLET, FILM COATED in 1 PACKET (58118-0712-0)
Product NDC
58118-0712
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
ANDA090278
Manufacturer
Clinical Solutions Wholesale
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/58118-0712-0