"68180-173-03" National Drug Code (NDC)

Topiramate 1000 TABLET in 1 BOTTLE (68180-173-03)
(Lupin Pharmaceuticals, Inc.)

NDC Code68180-173-03
Package Description1000 TABLET in 1 BOTTLE (68180-173-03)
Product NDC68180-173
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameTopiramate
Non-Proprietary NameTopiramate
Dosage FormTABLET
UsageORAL
Start Marketing Date20131109
Marketing Category NameANDA
Application NumberANDA078410
ManufacturerLupin Pharmaceuticals, Inc.
Substance NameTOPIRAMATE
Strength200
Strength Unitmg/1
Pharmacy ClassesDecreased Central Nervous System Disorganized Electrical Activity [PE],Cytochrome P450 3A4 Inducers [MoA],Cytochrome P450 2C19 Inhibitors [MoA]

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