Citalopram Hydrobromide
Citalopram Tablets, USP
Approved
Approval ID
3568b0ca-ba12-310b-e054-00144ff8d46c
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Jun 17, 2016
Manufacturers
FDA
Apotheca Inc.
DUNS: 051457844
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 Code12634-629
Application NumberANDA078216
Product Classification
M
Marketing Category
C73584
G
Generic Name
Citalopram Hydrobromide
Product Specifications
Route of AdministrationORAL
Effective DateJune 17, 2016
FDA Product Classification
INGREDIENTS (1)
CITALOPRAM HYDROBROMIDEActive
Quantity: 10 mg in 1 1
Code: I1E9D14F36
Classification: ACTIM