Fluoxetine

Product NDC

55700-617

11-digit product format

557000617

Labeler code

55700

Product ID

55700-617_295517ea-1856-4776-8b03-c5c56abdf726

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Fluoxetine

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

Lake Erie Medical DBA Quality Care Products LLC

Application

ANDA208698

Marketing category

ANDA

Marketing start

2018-05-11

Marketing end

0000-00-00

Substance

FLUOXETINE HYDROCHLORIDE

Active strength

10 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