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"47335-712-88" National Drug Code (NDC)
Topiramate 100 TABLET, FILM COATED in 1 BOTTLE (47335-712-88)
(Sun Pharmaceutical Industries, Inc.)
NDC Code
47335-712-88
Package Description
100 TABLET, FILM COATED in 1 BOTTLE (47335-712-88)
Product NDC
47335-712
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Topiramate
Non-Proprietary Name
Topiramate
Dosage Form
TABLET, FILM COATED
Usage
ORAL
Start Marketing Date
20141215
Marketing Category Name
ANDA
Application Number
ANDA090278
Manufacturer
Sun Pharmaceutical Industries, Inc.
Substance Name
TOPIRAMATE
Strength
200
Strength Unit
mg/1
Pharmacy Classes
Cytochrome P450 2C19 Inhibitors [MoA], Cytochrome P450 3A4 Inducers [MoA], Decreased Central Nervous System Disorganized Electrical Activity [PE]
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/47335-712-88