Sucralfate - 0093-2210-98 - (Sucralfate)

Alphabetical Index


Drug Information of Sucralfate

Product NDC: 0093-2210
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: 0093-2210
Labeler Name: Teva Pharmaceuticals USA Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA070848
Marketing Category: ANDA
Start Marketing Date: 19961111

Package Information of Sucralfate

Package NDC: 0093-2210-98
Package Description: 90 TABLET in 1 BOTTLE (0093-2210-98)

NDC Information of Sucralfate

NDC Code 0093-2210-98
Proprietary Name Sucralfate
Package Description 90 TABLET in 1 BOTTLE (0093-2210-98)
Product NDC 0093-2210
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Sucralfate
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19961111
Marketing Category Name ANDA
Labeler Name Teva Pharmaceuticals USA 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