"0603-1378-65" National Drug Code (NDC)

Lactulose 1892 mL in 1 BOTTLE (0603-1378-65)
(Par Pharmaceutical)

NDC Code0603-1378-65
Package Description1892 mL in 1 BOTTLE (0603-1378-65)
Product NDC0603-1378
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameLactulose
Non-Proprietary NameLactulose
Dosage FormSOLUTION
UsageORAL
Start Marketing Date20010726
End Marketing Date20191031
Marketing Category NameANDA
Application NumberANDA075993
ManufacturerPar Pharmaceutical
Substance NameLACTULOSE
Strength10
Strength Unitg/15mL
Pharmacy ClassesOsmotic Laxative [EPC],Osmotic Activity [MoA],Acidifying Activity [MoA],Stimulation Large Intestine Fluid/Electrolyte Secretion [PE]

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