NDC 65862-193 – Fluoxetine

Fluoxetine Hydrochloride 20 mg/1 · Capsule · Oral

Human Prescription Drug

Product NDC65862-193

Product details

Brand name
Fluoxetine
Generic name
Fluoxetine Hydrochloride
Labeler
Aurobindo Pharma Limited
Dosage form
Capsule
Route
Oral
Marketing category
ANDA · ANDA078619
Marketed since
January 31, 2008
Marketing end
February 29, 2028
Pharmacologic class
Serotonin Reuptake Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Fluoxetine →

Package NDC codes (2)

Package NDCDescriptionSince
65862-193-01100 CAPSULE in 1 BOTTLE (65862-193-01)Jan 31, 2018
65862-193-991000 CAPSULE in 1 BOTTLE (65862-193-99)Jan 31, 2018

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