Citalopram Hydrobromide
Citalopram Tablets, USP
Approved
Approval ID
c584909b-e7b2-7108-e053-2995a90a2f54
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Jun 24, 2021
Manufacturers
FDA
NuCare Pharmaceuticals,Inc.
DUNS: 010632300
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 Code68071-1830
Application NumberANDA078216
Product Classification
M
Marketing Category
C73584
G
Generic Name
Citalopram Hydrobromide
Product Specifications
Route of AdministrationORAL
Effective DateJune 24, 2021
FDA Product Classification
INGREDIENTS (1)
CITALOPRAM HYDROBROMIDEActive
Quantity: 20 mg in 1 1
Code: I1E9D14F36
Classification: ACTIM