PAROXETINE

Product NDC

70518-0964

11-digit product format

705180964

Labeler code

70518

Product ID

70518-0964_8f6ee50e-a8c2-24ba-e053-2995a90a68a2

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

paroxetine hydrochloride

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

REMEDYREPACK INC.

Application

ANDA075356

Marketing category

ANDA

Marketing start

2018-01-17

Marketing end

0000-00-00

Substance

PAROXETINE HYDROCHLORIDE ANHYDROUS

Active strength

10 mg/1

Pharmacologic classes

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

NDC exclude flag

No

Listing certified through

2020-12-31

Current FDA listing

Historical FDA.report record