ESCITALOPRAM
ESCITALOPRAM
Approved
Approval ID
0caa123d-3494-4443-afbe-5592f5c05b30
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Mar 25, 2015
Manufacturers
FDA
Northwind Pharmaceuticals, LLC
DUNS: 036986393
Products 1
Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.
escitalopram oxalate
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code51655-021
Application NumberANDA076765
Product Classification
M
Marketing Category
C73584
G
Generic Name
escitalopram oxalate
Product Specifications
Route of AdministrationORAL
Effective DateMarch 25, 2015
FDA Product Classification
INGREDIENTS (1)
ESCITALOPRAM OXALATEActive
Quantity: 10 mg in 1 1
Code: 5U85DBW7LO
Classification: ACTIM