Carafate - 58914-171-10 - (Sucralfate)

Alphabetical Index


Drug Information of Carafate

Product NDC: 58914-171
Proprietary Name: Carafate
Non Proprietary Name: Sucralfate
Active Ingredient(s): 1    g/1 & nbsp;   Sucralfate
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Carafate

Product NDC: 58914-171
Labeler Name: Aptalis Pharma US, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA018333
Marketing Category: NDA
Start Marketing Date: 19811030

Package Information of Carafate

Package NDC: 58914-171-10
Package Description: 100 TABLET in 1 BOTTLE (58914-171-10)

NDC Information of Carafate

NDC Code 58914-171-10
Proprietary Name Carafate
Package Description 100 TABLET in 1 BOTTLE (58914-171-10)
Product NDC 58914-171
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Sucralfate
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19811030
Marketing Category Name NDA
Labeler Name Aptalis Pharma US, Inc.
Substance Name SUCRALFATE
Strength Number 1
Strength Unit g/1
Pharmaceutical Classes Aluminum Complex [EPC],Organometallic Compounds [Chemical/Ingredient]

Complete Information of Carafate


General Information