FLUOXETINE

Product NDC

61919-340

11-digit product format

619190340

Labeler code

61919

Product ID

61919-340_5d50b3b3-cf1f-1d10-e053-2a91aa0a6de6

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

FLUOXETINE

Dosage form

CAPSULE

Route

ORAL

Labeler

DIRECT RX

Application

ANDA076001

Marketing category

ANDA

Marketing start

2017-11-06

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

E

Listing certified through

2018-12-31

Current FDA listing

Historical FDA.report record