SUCRALFATE - 54868-5299-1 - (Sucralfate)

Alphabetical Index


Drug Information of SUCRALFATE

Product NDC: 54868-5299
Proprietary Name: SUCRALFATE
Non Proprietary Name: Sucralfate
Active Ingredient(s): 1    g/10mL & nbsp;   Sucralfate
Administration Route(s): ORAL
Dosage Form(s): SUSPENSION
Coding System: National Drug Codes(NDC)

Labeler Information of SUCRALFATE

Product NDC: 54868-5299
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA019183
Marketing Category: NDA
Start Marketing Date: 20050524

Package Information of SUCRALFATE

Package NDC: 54868-5299-1
Package Description: 10 TRAY in 1 CASE (54868-5299-1) > 10 CUP, UNIT-DOSE in 1 TRAY > 10 mL in 1 CUP, UNIT-DOSE

NDC Information of SUCRALFATE

NDC Code 54868-5299-1
Proprietary Name SUCRALFATE
Package Description 10 TRAY in 1 CASE (54868-5299-1) > 10 CUP, UNIT-DOSE in 1 TRAY > 10 mL in 1 CUP, UNIT-DOSE
Product NDC 54868-5299
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Sucralfate
Dosage Form Name SUSPENSION
Route Name ORAL
Start Marketing Date 20050524
Marketing Category Name NDA
Labeler Name Physicians Total Care, Inc.
Substance Name SUCRALFATE
Strength Number 1
Strength Unit g/10mL
Pharmaceutical Classes Aluminum Complex [EPC],Organometallic Compounds [Chemical/Ingredient]

Complete Information of SUCRALFATE


General Information