Fluoxetine

Product NDC

35356-729

11-digit product format

353560729

Labeler code

35356

Product ID

35356-729_241f71be-cd89-42f6-9385-85e8086ec712

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

fluoxetine

Dosage form

CAPSULE

Route

ORAL

Labeler

Lake Erie Medical DBA Quality Care Products LLC

Application

ANDA076990

Marketing category

ANDA

Marketing start

2005-07-20

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

No

Listing certified through

2019-12-31

Current FDA listing

Historical FDA.report record