"66689-038-50" National Drug Code (NDC)

NDC Code	66689-038-50
Package Description	5 TRAY in 1 CASE (66689-038-50) / 10 CUP, UNIT-DOSE in 1 TRAY / 30 mL in 1 CUP, UNIT-DOSE (66689-038-01)
Product NDC	66689-038
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Lactulose
Non-Proprietary Name	Lactulose
Dosage Form	SOLUTION
Usage	ORAL
Start Marketing Date	20100510
End Marketing Date	20250531
Marketing Category Name	ANDA
Application Number	ANDA074138
Manufacturer	VistaPharm, LLC
Substance Name	LACTULOSE
Strength	20
Strength Unit	g/30mL
Pharmacy Classes	Acidifying Activity [MoA], Osmotic Activity [MoA], Osmotic Laxative [EPC], Stimulation Large Intestine Fluid/Electrolyte Secretion [PE]