Duloxetine

Product NDC

42708-021

11-digit product format

427080021

Labeler code

42708

Product ID

42708-021_eb8cd32d-83ad-4a78-aa6a-15718b3af7b2

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Duloxetine

Dosage form

CAPSULE, DELAYED RELEASE PELLETS

Route

ORAL

Labeler

QPharma Inc

Application

ANDA090783

Marketing category

ANDA

Marketing start

2013-12-11

Marketing end

0000-00-00

Substance

DULOXETINE HYDROCHLORIDE

Active strength

60 mg/1

Pharmacologic classes

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

NDC exclude flag

No

Listing certified through

2020-12-31

Current FDA listing

Historical FDA.report record