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"0093-7220-06" National Drug Code (NDC)
Topiramate 60 TABLET in 1 BOTTLE (0093-7220-06)
(Teva Pharmaceuticals USA Inc)
NDC Code
0093-7220-06
Package Description
60 TABLET in 1 BOTTLE (0093-7220-06)
Product NDC
0093-7220
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Topiramate
Non-Proprietary Name
Topiramate
Dosage Form
TABLET
Usage
ORAL
Start Marketing Date
20090331
End Marketing Date
20160229
Marketing Category Name
ANDA
Application Number
ANDA076317
Manufacturer
Teva Pharmaceuticals USA Inc
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/0093-7220-06