FLUOXETINE

Product NDC

50090-2568

11-digit product format

500902568

Labeler code

50090

Product ID

50090-2568_1d869aeb-3e2b-4520-85fe-56c2be97a92a

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

FLUOXETINE

Dosage form

CAPSULE

Route

ORAL

Labeler

A-S Medication Solutions

Application

ANDA204597

Marketing category

ANDA

Marketing start

2015-07-30

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