SERTRALINE HYDROCHLORIDE

Product NDC

55154-0532

11-digit product format

551540532

Labeler code

55154

Product ID

55154-0532_98982917-ad30-4c1c-aeee-ea925f17ebb5

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

sertraline hydrochloride

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

Cardinal Health

Application

NDA019839

Marketing category

NDA

Marketing start

1992-02-11

Marketing end

2019-04-30

Substance

SERTRALINE HYDROCHLORIDE

Active strength

100 mg/1

Pharmacologic classes

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

NDC exclude flag

No

Listing certified through

0000-00-00

Current FDA listing

Historical FDA.report record