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"68180-173-02" National Drug Code (NDC)
Topiramate 500 TABLET in 1 BOTTLE (68180-173-02)
(Lupin Pharmaceuticals, Inc.)
NDC Code
68180-173-02
Package Description
500 TABLET in 1 BOTTLE (68180-173-02)
Product NDC
68180-173
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Topiramate
Non-Proprietary Name
Topiramate
Dosage Form
TABLET
Usage
ORAL
Start Marketing Date
20131109
Marketing Category Name
ANDA
Application Number
ANDA078410
Manufacturer
Lupin Pharmaceuticals, 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/68180-173-02