Fluoxetine

Product NDC

68788-7409

11-digit product format

687887409

Labeler code

68788

Product ID

68788-7409_0fd80f1a-ca77-4cfc-a059-9ba38d2da496

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Fluoxetine Hydrochloride

Dosage form

CAPSULE

Route

ORAL

Labeler

Preferred Pharmaceuticals, Inc.

Application

ANDA204597

Marketing category

ANDA

Marketing start

2018-06-06

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

2020-12-31

Current FDA listing

Historical FDA.report record