Citalopram

Product NDC

71335-0656

11-digit product format

713350656

Labeler code

71335

Product ID

71335-0656_c49c933c-a3c7-43f3-b620-cd5698a690c9

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

citalopram hydrobromide

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

Bryant Ranch Prepack

Application

ANDA205407

Marketing category

ANDA

Marketing start

2015-12-23

Marketing end

0000-00-00

Substance

CITALOPRAM HYDROBROMIDE

Active strength

40 mg/1

Pharmacologic classes

Serotonin Reuptake Inhibitor [EPC],Serotonin Uptake Inhibitors [MoA]

NDC exclude flag

No

Listing certified through

2019-12-31

Current FDA listing

Historical FDA.report record