Lactulose - 17856-1378-1 - (lactulose)

Alphabetical Index


Drug Information of Lactulose

Product NDC: 17856-1378
Proprietary Name: Lactulose
Non Proprietary Name: lactulose
Active Ingredient(s): 10    g/15mL & nbsp;   lactulose
Administration Route(s): ORAL
Dosage Form(s): SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Lactulose

Product NDC: 17856-1378
Labeler Name: Atlantic Biologicals Corps
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075993
Marketing Category: ANDA
Start Marketing Date: 20010726

Package Information of Lactulose

Package NDC: 17856-1378-1
Package Description: 30 mL in 1 CUP (17856-1378-1)

NDC Information of Lactulose

NDC Code 17856-1378-1
Proprietary Name Lactulose
Package Description 30 mL in 1 CUP (17856-1378-1)
Product NDC 17856-1378
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name lactulose
Dosage Form Name SOLUTION
Route Name ORAL
Start Marketing Date 20010726
Marketing Category Name ANDA
Labeler Name Atlantic Biologicals Corps
Substance Name LACTULOSE
Strength Number 10
Strength Unit g/15mL
Pharmaceutical Classes Osmotic Laxative [EPC],Osmotic Activity [MoA],Acidifying Activity [MoA],Stimulation Large Intestine Fluid/Electrolyte Secretion [PE]

Complete Information of Lactulose


General Information