Fluoxetine Hydrochloride

Product NDC

0615-1387

11-digit product format

006151387

Labeler code

0615

Product ID

0615-1387_8e35dc0e-bf0e-49d8-b5a7-7b76d5829795

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Fluoxetine Hydrochloride

Dosage form

CAPSULE

Route

ORAL

Labeler

NCS HealthCare of KY, Inc dba Vangard Labs

Application

ANDA075049

Marketing category

ANDA

Marketing start

2002-01-29

Marketing end

0000-00-00

Substance

FLUOXETINE HYDROCHLORIDE

Active strength

40 mg/1

Pharmacologic classes

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

NDC exclude flag

E

Listing certified through

2017-12-31

Current FDA listing

Historical FDA.report record