Fluoxetine

Product NDC

55700-177

11-digit product format

557000177

Labeler code

55700

Product ID

55700-177_474af8ca-01e2-4e29-822a-9cf07f143185

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Fluoxetine

Dosage form

CAPSULE

Route

ORAL

Labeler

Lake Erie Medical DBA Quality Care Products LLC

Application

ANDA076001

Marketing category

ANDA

Marketing start

2002-01-29

Marketing end

0000-00-00

Substance

FLUOXETINE HYDROCHLORIDE

Active strength

20 mg/1

Pharmacologic classes

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

NDC exclude flag

No

Listing certified through

2020-12-31

Current FDA listing

Historical FDA.report record