"16571-706-10" National Drug Code (NDC)

Topiramate 1000 TABLET, FILM COATED in 1 BOTTLE (16571-706-10)
(Rising Pharma Holdings, Inc.)

NDC Code16571-706-10
Package Description1000 TABLET, FILM COATED in 1 BOTTLE (16571-706-10)
Product NDC16571-706
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameTopiramate
Non-Proprietary NameTopiramate
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20090327
Marketing Category NameANDA
Application NumberANDA078462
ManufacturerRising Pharma Holdings, Inc.
Substance NameTOPIRAMATE
Strength50
Strength Unitmg/1
Pharmacy ClassesCytochrome P450 2C19 Inhibitors [MoA], Cytochrome P450 3A4 Inducers [MoA], Decreased Central Nervous System Disorganized Electrical Activity [PE]

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