SUCRALFATE
SUCRALFATE SUSPENSION1 g/10 mL
Approved
Approval ID
187ce680-e3de-45cb-98f3-96e069804c62
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Nov 24, 2010
Manufacturers
FDA
Physicians Total Care, Inc.
DUNS: 194123980
Products 1
Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.
Sucralfate
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code54868-5299
Application NumberNDA019183
Product Classification
M
Marketing Category
C73594
G
Generic Name
Sucralfate
Product Specifications
Route of AdministrationORAL
Effective DateApril 1, 2011
FDA Product Classification
INGREDIENTS (7)
SILICON DIOXIDEInactive
Code: ETJ7Z6XBU4
Classification: IACT
SUCRALFATEActive
Quantity: 1 g in 10 mL
Code: XX73205DH5
Classification: ACTIB
FD&C RED NO. 40Inactive
Code: WZB9127XOA
Classification: IACT
WATERInactive
Code: 059QF0KO0R
Classification: IACT
CELLULOSE, MICROCRYSTALLINEInactive
Code: OP1R32D61U
Classification: IACT
GLYCERINInactive
Code: PDC6A3C0OX
Classification: IACT
SORBITOLInactive
Code: 506T60A25R
Classification: IACT