Citalopram

Product NDC

0185-0371

11-digit product format

001850371

Labeler code

0185

Product ID

0185-0371_7135ba86-24ce-4783-aebd-1768afcb40a0

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Citalopram Hydrobromide

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

Eon Labs, Inc.

Application

ANDA077031

Marketing category

ANDA

Marketing start

2004-10-28

Marketing end

0000-00-00

Substance

CITALOPRAM HYDROBROMIDE

Active strength

10 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