Sucralfate - 54868-3933-1 - (Sucralfate)

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Drug Information of Sucralfate

Product NDC: 54868-3933
Proprietary Name: Sucralfate
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 Sucralfate

Product NDC: 54868-3933
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA070848
Marketing Category: ANDA
Start Marketing Date: 20050523

Package Information of Sucralfate

Package NDC: 54868-3933-1
Package Description: 60 TABLET in 1 BOTTLE (54868-3933-1)

NDC Information of Sucralfate

NDC Code 54868-3933-1
Proprietary Name Sucralfate
Package Description 60 TABLET in 1 BOTTLE (54868-3933-1)
Product NDC 54868-3933
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Sucralfate
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20050523
Marketing Category Name ANDA
Labeler Name Physicians Total Care, Inc.
Substance Name SUCRALFATE
Strength Number 1
Strength Unit g/1
Pharmaceutical Classes Aluminum Complex [EPC],Organometallic Compounds [Chemical/Ingredient]

Complete Information of Sucralfate


General Information