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"47335-712-18" National Drug Code (NDC)

Topiramate 1000 TABLET, FILM COATED in 1 BOTTLE (47335-712-18)
(Sun Pharmaceutical Industries, Inc.)

NDC Code47335-712-18
Package Description1000 TABLET, FILM COATED in 1 BOTTLE (47335-712-18)
Product NDC47335-712
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameTopiramate
Non-Proprietary NameTopiramate
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20141215
Marketing Category NameANDA
Application NumberANDA090278
ManufacturerSun Pharmaceutical Industries, Inc.
Substance NameTOPIRAMATE
Strength200
Strength Unitmg/1
Pharmacy ClassesCytochrome 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/47335-712-18





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