Sucralfate - 49349-408-02 - (Sucralfate)

Alphabetical Index


Drug Information of Sucralfate

Product NDC: 49349-408
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: 49349-408
Labeler Name: REMEDYREPACK INC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA018333
Marketing Category: NDA
Start Marketing Date: 20110721

Package Information of Sucralfate

Package NDC: 49349-408-02
Package Description: 30 TABLET in 1 BLISTER PACK (49349-408-02)

NDC Information of Sucralfate

NDC Code 49349-408-02
Proprietary Name Sucralfate
Package Description 30 TABLET in 1 BLISTER PACK (49349-408-02)
Product NDC 49349-408
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Sucralfate
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20110721
Marketing Category Name NDA
Labeler Name REMEDYREPACK 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