Citalopram

Product NDC

55700-356

11-digit product format

557000356

Labeler code

55700

Product ID

55700-356_a5765fb0-8f5b-402b-8bfc-e1233785a60e

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Citalopram Hydrobromide

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

Lake Erie Medical DBA Quality Care Products LLC

Application

ANDA077031

Marketing category

ANDA

Marketing start

2004-10-28

Marketing end

0000-00-00

Substance

CITALOPRAM HYDROBROMIDE

Active strength

20 mg/1

Pharmacologic classes

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

NDC exclude flag

No

Listing certified through

2020-12-31

Current FDA listing

Historical FDA.report record