Fluoxetine

Product NDC

55700-593

11-digit product format

557000593

Labeler code

55700

Product ID

55700-593_8e1c5c71-0f26-4027-a530-37af395d6c4c

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Fluoxetine Hydrochloride

Dosage form

CAPSULE

Route

ORAL

Labeler

Lake Erie Medical DBA Quality Care Products LLC

Application

ANDA204597

Marketing category

ANDA

Marketing start

2015-03-16

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