NDC 50090-7225 – Fluoxetine

Fluoxetine Hydrochloride 20 mg/1 · Capsule · Oral

Human Prescription Drug

Product NDC50090-7225

Product details

Brand name
Fluoxetine
Generic name
Fluoxetine Hydrochloride
Labeler
A-S Medication Solutions
Dosage form
Capsule
Route
Oral
Marketing category
ANDA · ANDA204597
Marketed since
March 16, 2015
Listing expires
December 31, 2026
Pharmacologic class
Serotonin Reuptake Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Fluoxetine →

Package NDC codes (3)

Package NDCDescriptionSince
50090-7225-030 CAPSULE in 1 BOTTLE (50090-7225-0)Aug 20, 2024
50090-7225-160 CAPSULE in 1 BOTTLE (50090-7225-1)Aug 20, 2024
50090-7225-390 CAPSULE in 1 BOTTLE (50090-7225-3)Aug 20, 2024

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