Sertraline hydrochloride

Product NDC

13668-006

11-digit product format

136680006

Labeler code

13668

Product ID

13668-006_a2f71c11-af32-4d43-beac-87af9f76afc7

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Sertraline hydrochloride

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

Torrent Pharmaceuticals Limited

Application

ANDA077765

Marketing category

ANDA

Marketing start

2007-09-05

Marketing end

0000-00-00

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

2019-12-31

Current FDA listing

Historical FDA.report record