Sucralfate - 63629-1307-8 - (Sucralfate)

Alphabetical Index


Drug Information of Sucralfate

Product NDC: 63629-1307
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: 63629-1307
Labeler Name: Bryant Ranch Prepack
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA070848
Marketing Category: ANDA
Start Marketing Date: 20100108

Package Information of Sucralfate

Package NDC: 63629-1307-8
Package Description: 40 TABLET in 1 BOTTLE (63629-1307-8)

NDC Information of Sucralfate

NDC Code 63629-1307-8
Proprietary Name Sucralfate
Package Description 40 TABLET in 1 BOTTLE (63629-1307-8)
Product NDC 63629-1307
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Sucralfate
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20100108
Marketing Category Name ANDA
Labeler Name Bryant Ranch Prepack
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