Fluoxetine Hydrochloride

Product NDC

70518-0170

11-digit product format

705180170

Labeler code

70518

Product ID

70518-0170_9f645b99-a910-8336-e053-2a95a90a9c11

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Fluoxetine Hydrochloride

Dosage form

CAPSULE

Route

ORAL

Labeler

REMEDYREPACK INC.

Application

ANDA075049

Marketing category

ANDA

Marketing start

2017-01-23

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

2021-12-31

Current FDA listing

Historical FDA.report record