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"16571-707-10" National Drug Code (NDC)
Topiramate 1000 TABLET, FILM COATED in 1 BOTTLE (16571-707-10)
(Rising Pharma Holdings, Inc.)
NDC Code
16571-707-10
Package Description
1000 TABLET, FILM COATED in 1 BOTTLE (16571-707-10)
Product NDC
16571-707
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
ANDA078462
Manufacturer
Rising Pharma Holdings, Inc.
Substance Name
TOPIRAMATE
Strength
100
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/16571-707-10