Citalopram Hydrobromide

Product NDC

68462-114

11-digit product format

684620114

Labeler code

68462

Product ID

68462-114_a2e433a6-ad8c-48d9-b52a-398b1168a053

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Citalopram Hydrobromide

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

Glenmark Generics Inc., USA

Application

ANDA077654

Marketing category

ANDA

Marketing start

2009-02-27

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

E

Listing certified through

2018-12-31

Current FDA listing

Historical FDA.report record