SUCRALFATE - 16590-523-72 - (SUCRALFATE)

Alphabetical Index


Drug Information of SUCRALFATE

Product NDC: 16590-523
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: 16590-523
Labeler Name: STAT RX USA LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA074415
Marketing Category: ANDA
Start Marketing Date: 20090701

Package Information of SUCRALFATE

Package NDC: 16590-523-72
Package Description: 120 TABLET in 1 BOTTLE, PLASTIC (16590-523-72)

NDC Information of SUCRALFATE

NDC Code 16590-523-72
Proprietary Name SUCRALFATE
Package Description 120 TABLET in 1 BOTTLE, PLASTIC (16590-523-72)
Product NDC 16590-523
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name SUCRALFATE
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20090701
Marketing Category Name ANDA
Labeler Name STAT RX USA LLC
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