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"0093-7219-10" National Drug Code (NDC)

Topiramate 1000 TABLET in 1 BOTTLE (0093-7219-10)
(Teva Pharmaceuticals USA Inc)

NDC Code0093-7219-10
Package Description1000 TABLET in 1 BOTTLE (0093-7219-10)
Product NDC0093-7219
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameTopiramate
Non-Proprietary NameTopiramate
Dosage FormTABLET
UsageORAL
Start Marketing Date20090331
End Marketing Date20160731
Marketing Category NameANDA
Application NumberANDA076317
ManufacturerTeva Pharmaceuticals USA Inc
Substance NameTOPIRAMATE
Strength100
Strength Unitmg/1
Pharmacy ClassesDecreased 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/0093-7219-10





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