Citalopram Hydrobromide
Citalopram Tablets USP
Approved
Approval ID
789d1ece-181b-4eca-b449-f15b6071de90
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Sep 22, 2011
Manufacturers
FDA
MedVantx, Inc.
DUNS: 806427725
Products 1
Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.
Citalopram Hydrobromide
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code66116-405
Application NumberANDA078216
Product Classification
M
Marketing Category
C73584
G
Generic Name
Citalopram Hydrobromide
Product Specifications
Route of AdministrationORAL
Effective DateSeptember 22, 2011
FDA Product Classification
INGREDIENTS (1)
CITALOPRAM HYDROBROMIDEActive
Quantity: 20 mg in 1 1
Code: I1E9D14F36
Classification: ACTIM