Prozac

Product NDC

0002-3004

11-digit product format

000023004

Labeler code

0002

Product ID

0002-3004_f1404e9d-0c95-44e4-9eb0-7a2836a67bd8

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Fluoxetine hydrochloride

Dosage form

CAPSULE, DELAYED RELEASE

Route

ORAL

Labeler

Eli Lilly and Company

Application

NDA021235

Marketing category

NDA

Marketing start

2001-03-16

Marketing end

0000-00-00

Substance

FLUOXETINE HYDROCHLORIDE

Active strength

90 mg/1

Pharmacologic classes

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

NDC exclude flag

No

Listing certified through

2019-12-31

Current FDA listing

Historical FDA.report record