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"61786-732-02" National Drug Code (NDC)
Topiramate 30 TABLET, FILM COATED in 1 BLISTER PACK (61786-732-02)
(REMEDYREPACK INC.)
NDC Code
61786-732-02
Package Description
30 TABLET, FILM COATED in 1 BLISTER PACK (61786-732-02)
Product NDC
61786-732
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Topiramate
Non-Proprietary Name
Topiramate
Dosage Form
TABLET, FILM COATED
Usage
ORAL
Start Marketing Date
20160607
Marketing Category Name
ANDA
Application Number
ANDA078235
Manufacturer
REMEDYREPACK INC.
Substance Name
TOPIRAMATE
Strength
100
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/61786-732-02