Fluoxetine Hydrochloride

Product NDC

55700-808

11-digit product format

557000808

Labeler code

55700

Product ID

55700-808_c0f6fe3d-2800-4cc8-b176-21dcdea69aa5

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Fluoxetine Hydrochloride

Dosage form

TABLET

Route

ORAL

Labeler

Quality Care Products, LLC

Application

ANDA211653

Marketing category

ANDA

Marketing start

2019-10-18

Marketing end

0000-00-00

Substance

FLUOXETINE HYDROCHLORIDE

Active strength

10 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