Duloxetine

Product NDC

50090-3028

11-digit product format

500903028

Labeler code

50090

Product ID

50090-3028_8fd00bfa-3083-49f3-bcfe-4186dda403e5

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

DULOXETINE HYDROCHLORIDE

Dosage form

CAPSULE, DELAYED RELEASE PELLETS

Route

ORAL

Labeler

A-S Medication Solutions

Application

ANDA203088

Marketing category

ANDA

Marketing start

2014-06-11

Marketing end

0000-00-00

Substance

DULOXETINE HYDROCHLORIDE

Active strength

20 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