Duloxetine

Product NDC

50090-2517

11-digit product format

500902517

Labeler code

50090

Product ID

50090-2517_5ee4cf9a-f3e6-4151-9851-ebe987dc4dad

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Duloxetine

Dosage form

CAPSULE, DELAYED RELEASE PELLETS

Route

ORAL

Labeler

A-S Medication Solutions

Application

ANDA090776

Marketing category

ANDA

Marketing start

2013-12-17

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