Fluoxetine

Product NDC

50268-334

11-digit product format

502680334

Labeler code

50268

Product ID

50268-334_6ad7438d-5af8-d2a5-e053-2991aa0afb52

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Fluoxetine Hydrochloride

Dosage form

CAPSULE

Route

ORAL

Labeler

AvPAK

Application

ANDA078619

Marketing category

ANDA

Marketing start

2014-08-20

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

2019-12-31

Current FDA listing

Historical FDA.report record