NDC 84386-105 – Fluoxetine

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

Human Prescription Drug

Product NDC84386-105

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
January 15, 2026
Listing expires
December 31, 2027
Pharmacologic class
Serotonin Reuptake Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Fluoxetine →

Package NDC codes (2)

Package NDCDescriptionSince
84386-105-01100 TABLET, FILM COATED in 1 BOTTLE (84386-105-01)Jan 15, 2026
84386-105-3030 TABLET, FILM COATED in 1 BOTTLE (84386-105-30)Jan 15, 2026

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