DESLORATADINE
These highlights do not include all the information needed to use DESLORATADINE TABLETS safely and effectively. See full prescribing information for DESLORATADINE TABLETS. DESLORATADINE tablets for oral use Initial U.S. Approval: 2001
Approved
Approval ID
f84c8de3-a7d3-4e8b-bfb6-04259e79450a
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Jan 19, 2020
Manufacturers
FDA
Bryant Ranch Prepack
DUNS: 171714327
Products 1
Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.
DESLORATADINE
PRODUCT DETAILS
NDC Product Code71335-1000
Application NumberANDA078352
Marketing CategoryC73584
Route of AdministrationORAL
Effective DateApril 19, 2019
Generic NameDESLORATADINE
INGREDIENTS (1)
DESLORATADINEActive
Quantity: 5 mg in 1 1
Code: FVF865388R
Classification: ACTIB