MedPath
FDA Product

Fluoxetine

Product approved by U.S. Food and Drug Administration (US)

Basic Information

Fluoxetine

71335-2020

Regulatory Information

71335-2020

ANDA204597

C73584

May 25, 2023

USA

These highlights do not include all the information needed to use FLUOXETINE CAPSULES, safely and effectively. See full prescribing information for FLUOXETINE CAPSULES. FLUOXETINE capsules, for oral use Initial U.S. Approval: 1987

HUMAN PRESCRIPTION DRUG LABEL

101

Company Information

171714327

Active Ingredients

STARCH, CORN

Code: O8232NY3SJ

Class Code: IACT

SILICON DIOXIDE

Code: ETJ7Z6XBU4

Class Code: IACT

FD&C BLUE NO. 1

Code: H3R47K3TBD

Class Code: IACT

GELATIN, UNSPECIFIED

Code: 2G86QN327L

Class Code: IACT

SODIUM LAURYL SULFATE

Code: 368GB5141J

Class Code: IACT

FD&C RED NO. 3

Code: PN2ZH5LOQY

Class Code: IACT

TITANIUM DIOXIDE

Code: 15FIX9V2JP

Class Code: IACT

D&C YELLOW NO. 10

Code: 35SW5USQ3G

Class Code: IACT

FERROSOFERRIC OXIDE

Code: XM0M87F357

Class Code: IACT

POTASSIUM HYDROXIDE

Code: WZH3C48M4T

Class Code: IACT

PROPYLENE GLYCOL

Code: 6DC9Q167V3

Class Code: IACT

SHELLAC

Code: 46N107B71O

Class Code: IACT

FLUOXETINE HYDROCHLORIDE

Quantity: 20 mg in 1 1

Code: I9W7N6B1KJ

Class Code: ACTIM

AMMONIA

Code: 5138Q19F1X

Class Code: IACT

Active Moieties

FLUOXETINE

Code: 01K63SUP8D

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