Cymbalta

Product NDC

49999-618

11-digit product format

499990618

Labeler code

49999

Product ID

49999-618_ffc7083a-3b21-43e0-b134-398e86c47f0f

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Duloxetine hydrochloride

Dosage form

CAPSULE, DELAYED RELEASE

Route

ORAL

Labeler

Lake Erie Medical Surgical & Supply DBA Quality Care Products LLC

Application

NDA021427

Marketing category

NDA

Marketing start

2011-07-14

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