Lactulose - 54868-3101-1 - (lactulose)

Alphabetical Index


Drug Information of Lactulose

Product NDC: 54868-3101
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: 54868-3101
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA074623
Marketing Category: ANDA
Start Marketing Date: 20040419

Package Information of Lactulose

Package NDC: 54868-3101-1
Package Description: 473 mL in 1 BOTTLE (54868-3101-1)

NDC Information of Lactulose

NDC Code 54868-3101-1
Proprietary Name Lactulose
Package Description 473 mL in 1 BOTTLE (54868-3101-1)
Product NDC 54868-3101
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name lactulose
Dosage Form Name SOLUTION
Route Name ORAL
Start Marketing Date 20040419
Marketing Category Name ANDA
Labeler Name Physicians Total Care, Inc.
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