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
2a90b899-7746-43dc-ac8a-e754428eb30c
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Jan 19, 2024
Manufacturers
FDA
Lupin Pharmaceuticals, Inc.
DUNS: 089153071
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 Code68180-153
Application NumberANDA078352
Marketing CategoryC73584
Route of AdministrationORAL
Effective DateJanuary 19, 2024
Generic NameDESLORATADINE
INGREDIENTS (1)
DESLORATADINEActive
Quantity: 5 mg in 1 1
Code: FVF865388R
Classification: ACTIB