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"69097-819-12" National Drug Code (NDC)
Topiramate 500 TABLET in 1 BOTTLE (69097-819-12)
(Cipla USA Inc.)
NDC Code
69097-819-12
Package Description
500 TABLET in 1 BOTTLE (69097-819-12)
Product NDC
69097-819
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Topiramate
Non-Proprietary Name
Topiramate
Dosage Form
TABLET
Usage
ORAL
Start Marketing Date
20160722
Marketing Category Name
ANDA
Application Number
ANDA079162
Manufacturer
Cipla USA 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/69097-819-12