"50383-779-32" National Drug Code (NDC)

Lactulose 946 mL in 1 BOTTLE (50383-779-32)
(Akorn)

NDC Code50383-779-32
Package Description946 mL in 1 BOTTLE (50383-779-32)
Product NDC50383-779
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameLactulose
Non-Proprietary NameLactulose
Dosage FormSOLUTION
UsageORAL
Start Marketing Date19950703
Marketing Category NameANDA
Application NumberANDA074076
ManufacturerAkorn
Substance NameLACTULOSE
Strength10
Strength Unitg/15mL
Pharmacy ClassesAcidifying Activity [MoA], Osmotic Activity [MoA], Osmotic Laxative [EPC], Stimulation Large Intestine Fluid/Electrolyte Secretion [PE]

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