SUCRALFATE
Approved
Approval ID
c7e61193-6f73-4ae6-9560-ff23003b959b
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Feb 19, 2010
Manufacturers
FDA
STAT RX USA LLC
DUNS: 786036330
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 Code16590-523
Application NumberANDA074415
Product Classification
M
Marketing Category
C73584
G
Generic Name
SUCRALFATE
Product Specifications
Route of AdministrationORAL
Effective DateFebruary 19, 2010
FDA Product Classification
INGREDIENTS (1)
SUCRALFATEActive
Quantity: 1 g in 1 1
Code: XX73205DH5
Classification: ACTIB