"72205-084-30" National Drug Code (NDC)

Tiagabine Hydrochloride 30 TABLET in 1 BOTTLE (72205-084-30)
(Novadoz Pharmaceuticals LLC)

NDC Code72205-084-30
Package Description30 TABLET in 1 BOTTLE (72205-084-30)
Product NDC72205-084
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameTiagabine Hydrochloride
Non-Proprietary NameTiagabine Hydrochloride
Dosage FormTABLET
UsageORAL
Start Marketing Date20211123
Marketing Category NameANDA
Application NumberANDA214816
ManufacturerNovadoz Pharmaceuticals LLC
Substance NameTIAGABINE HYDROCHLORIDE
Strength2
Strength Unitmg/1
Pharmacy ClassesAnti-epileptic Agent [EPC], Decreased Central Nervous System Disorganized Electrical Activity [PE]

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