"69097-819-12" National Drug Code (NDC)

Topiramate 500 TABLET in 1 BOTTLE (69097-819-12)
(Cipla USA Inc.)

NDC Code69097-819-12
Package Description500 TABLET in 1 BOTTLE (69097-819-12)
Product NDC69097-819
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameTopiramate
Non-Proprietary NameTopiramate
Dosage FormTABLET
UsageORAL
Start Marketing Date20160722
Marketing Category NameANDA
Application NumberANDA079162
ManufacturerCipla USA 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]

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