Citalopram

Product NDC

68071-4291

11-digit product format

680714291

Labeler code

68071

Product ID

68071-4291_65932d9b-48fa-76ab-e053-2a91aa0a6ef5

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

citalopram hydrobromide

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

NuCare Pharmaceuticals,Inc.

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