"51672-4186-1" National Drug Code (NDC)

Felbamate 100 TABLET in 1 BOTTLE (51672-4186-1)
(Sun Pharmaceutical Industries, Inc.)

NDC Code51672-4186-1
Package Description100 TABLET in 1 BOTTLE (51672-4186-1)
Product NDC51672-4186
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameFelbamate
Non-Proprietary NameFelbamate
Dosage FormTABLET
UsageORAL
Start Marketing Date20170420
Marketing Category NameANDA
Application NumberANDA207093
ManufacturerSun Pharmaceutical Industries, Inc.
Substance NameFELBAMATE
Strength600
Strength Unitmg/1
Pharmacy ClassesAnti-epileptic Agent [EPC], Decreased Central Nervous System Disorganized Electrical Activity [PE]

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