Duloxetine

Product NDC

70518-1137

11-digit product format

705181137

Labeler code

70518

Product ID

70518-1137_6ab50c3f-2f81-5972-e053-2991aa0ae11e

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Duloxetine

Dosage form

CAPSULE, DELAYED RELEASE

Route

ORAL

Labeler

REMEDYREPACK INC.

Application

ANDA090745

Marketing category

ANDA

Marketing start

2018-04-25

Marketing end

0000-00-00

Substance

DULOXETINE HYDROCHLORIDE

Active strength

30 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

2019-12-31

Current FDA listing

Historical FDA.report record