Paroxetine

Product NDC

68788-6985

11-digit product format

687886985

Labeler code

68788

Product ID

68788-6985_1ef626e0-d347-4453-9c71-d90748a66922

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

paroxetine hydrochloride

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

Preferred Pharmaceuticals Inc.

Application

ANDA203854

Marketing category

ANDA

Marketing start

2017-07-05

Marketing end

0000-00-00

Substance

PAROXETINE HYDROCHLORIDE ANHYDROUS

Active strength

20 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