"62135-002-47" National Drug Code (NDC)

NDC Code	62135-002-47
Package Description	473 mL in 1 PACKAGE (62135-002-47)
Product NDC	62135-002
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Lactulose
Non-Proprietary Name	Lactulose
Dosage Form	SOLUTION
Usage	ORAL
Start Marketing Date	20181123
Marketing Category Name	ANDA
Application Number	ANDA209517
Manufacturer	Chartwell RX, LLC
Substance Name	LACTULOSE
Strength	10
Strength Unit	g/15mL
Pharmacy Classes	Acidifying Activity [MoA], Osmotic Activity [MoA], Osmotic Laxative [EPC], Stimulation Large Intestine Fluid/Electrolyte Secretion [PE]