NDC 59651-309 – Fluoxetine

Fluoxetine Hydrochloride 20 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC59651-309

Product details

Brand name
Fluoxetine
Generic name
Fluoxetine
Labeler
Aurobindo Pharma Limited
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA213286
Marketed since
April 8, 2020
Listing expires
December 31, 2026
Pharmacologic class
Serotonin Reuptake Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Fluoxetine →

Package NDC codes (2)

Package NDCDescriptionSince
59651-309-01100 TABLET, FILM COATED in 1 BOTTLE (59651-309-01)Apr 8, 2020
59651-309-3030 TABLET, FILM COATED in 1 BOTTLE (59651-309-30)Apr 8, 2020

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