Sertraline

Product NDC

70518-0240

11-digit product format

705180240

Labeler code

70518

Product ID

70518-0240_9fdd6f30-f3c3-6fb1-e053-2a95a90a95ca

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Sertraline

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

REMEDYREPACK INC.

Application

ANDA077670

Marketing category

ANDA

Marketing start

2017-02-20

Marketing end

0000-00-00

Substance

SERTRALINE HYDROCHLORIDE

Active strength

50 mg/1

Pharmacologic classes

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

NDC exclude flag

No

Listing certified through

2021-12-31

Current FDA listing

Historical FDA.report record