Sucralfate - 55154-9432-5 - (Sucralfate)

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Drug Information of Sucralfate

Product NDC: 55154-9432
Proprietary Name: Sucralfate
Non Proprietary Name: Sucralfate
Active Ingredient(s): 1    g/10mL & nbsp;   Sucralfate
Administration Route(s): ORAL
Dosage Form(s): SUSPENSION
Coding System: National Drug Codes(NDC)

Labeler Information of Sucralfate

Product NDC: 55154-9432
Labeler Name: Cardinal Health
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA019183
Marketing Category: NDA
Start Marketing Date: 20091119

Package Information of Sucralfate

Package NDC: 55154-9432-5
Package Description: 5 CUP, UNIT-DOSE in 1 BAG (55154-9432-5) > 10 mL in 1 CUP, UNIT-DOSE

NDC Information of Sucralfate

NDC Code 55154-9432-5
Proprietary Name Sucralfate
Package Description 5 CUP, UNIT-DOSE in 1 BAG (55154-9432-5) > 10 mL in 1 CUP, UNIT-DOSE
Product NDC 55154-9432
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Sucralfate
Dosage Form Name SUSPENSION
Route Name ORAL
Start Marketing Date 20091119
Marketing Category Name NDA
Labeler Name Cardinal Health
Substance Name SUCRALFATE
Strength Number 1
Strength Unit g/10mL
Pharmaceutical Classes Aluminum Complex [EPC],Organometallic Compounds [Chemical/Ingredient]

Complete Information of Sucralfate


General Information