Citalopram Hydrobromide
Citalopram Tablets, USP
Approved
Approval ID
39537c48-cf79-4137-bc29-4be9844bdd86
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Aug 17, 2022
Manufacturers
FDA
Quality Care Products, LLC
DUNS: 831276758
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 Code55700-838
Application NumberANDA078216
Product Classification
M
Marketing Category
C73584
G
Generic Name
Citalopram Hydrobromide
Product Specifications
Route of AdministrationORAL
Effective DateJanuary 30, 2020
FDA Product Classification
INGREDIENTS (1)
CITALOPRAM HYDROBROMIDEActive
Quantity: 40 mg in 1 1
Code: I1E9D14F36
Classification: ACTIM