Kristalose - 66220-729-30 - (lactulose)

Alphabetical Index


Drug Information of Kristalose

Product NDC: 66220-729
Proprietary Name: Kristalose
Non Proprietary Name: lactulose
Active Ingredient(s): 20    g/20g & nbsp;   lactulose
Administration Route(s): ORAL
Dosage Form(s): POWDER, FOR SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Kristalose

Product NDC: 66220-729
Labeler Name: Cumberland Pharmaceuticals Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA074712
Marketing Category: ANDA
Start Marketing Date: 20120120

Package Information of Kristalose

Package NDC: 66220-729-30
Package Description: 30 POUCH in 1 CARTON (66220-729-30) > 20 g in 1 POUCH (66220-729-01)

NDC Information of Kristalose

NDC Code 66220-729-30
Proprietary Name Kristalose
Package Description 30 POUCH in 1 CARTON (66220-729-30) > 20 g in 1 POUCH (66220-729-01)
Product NDC 66220-729
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name lactulose
Dosage Form Name POWDER, FOR SOLUTION
Route Name ORAL
Start Marketing Date 20120120
Marketing Category Name ANDA
Labeler Name Cumberland Pharmaceuticals Inc.
Substance Name LACTULOSE
Strength Number 20
Strength Unit g/20g
Pharmaceutical Classes Osmotic Laxative [EPC],Osmotic Activity [MoA],Acidifying Activity [MoA],Stimulation Large Intestine Fluid/Electrolyte Secretion [PE]

Complete Information of Kristalose


General Information