Sertraline

Product NDC

51655-979

11-digit product format

516550979

Labeler code

51655

Product ID

51655-979_49f0a12e-3c5b-4706-a247-f35708794fa6

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Sertraline

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

Northwind Pharmaceuticals

Application

ANDA077670

Marketing category

ANDA

Marketing start

2014-05-27

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

E

Listing certified through

2018-12-31

Current FDA listing

Historical FDA.report record