Citalopram
CITALOPRAM TABLETS USP 4740 4741 4742 Rx only
Approved
Approval ID
5665e444-b914-460d-a023-8a241c18cbb6
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Jul 18, 2013
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
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code66116-455
Application NumberANDA077048
Product Classification
M
Marketing Category
C73584
G
Generic Name
Citalopram
Product Specifications
Route of AdministrationORAL
Effective DateJuly 18, 2013
FDA Product Classification
INGREDIENTS (7)
STARCH, CORNInactive
Code: O8232NY3SJ
Classification: IACT
CITALOPRAM HYDROBROMIDEActive
Quantity: 40 mg in 1 1
Code: I1E9D14F36
Classification: ACTIM
CROSCARMELLOSE SODIUMInactive
Code: M28OL1HH48
Classification: IACT
LACTOSE MONOHYDRATEInactive
Code: EWQ57Q8I5X
Classification: IACT
MAGNESIUM STEARATEInactive
Code: 70097M6I30
Classification: IACT
CELLULOSE, MICROCRYSTALLINEInactive
Code: OP1R32D61U
Classification: IACT
POVIDONE K30Inactive
Code: U725QWY32X
Classification: IACT