FLUOXETINE

Product NDC

66267-587

11-digit product format

662670587

Labeler code

66267

Product ID

66267-587_9cc084de-7066-5560-e053-2a95a90a69a9

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

FLUOXETINE

Dosage form

CAPSULE

Route

ORAL

Labeler

NuCarePharmaceuticals, Inc.

Application

ANDA204597

Marketing category

ANDA

Marketing start

2015-07-30

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

2021-12-31

Current FDA listing

Historical FDA.report record