PAROXETINE HYDROCHLORIDE ANHYDROUS

Product NDC

61919-181

11-digit product format

619190181

Labeler code

61919

Product ID

61919-181_45a15eec-c38f-4825-9566-2d5c88d41d52

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

PAROXETINE HYDROCHLORIDE ANHYDROUS

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

DIRECT RX

Application

ANDA075356

Marketing category

ANDA

Marketing start

2014-01-01

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

2017-12-31

Current FDA listing

Historical FDA.report record