NDC 0121-4721 – Fluoxetine

Fluoxetine Hydrochloride 20 mg/5mL · Solution · Oral

Human Prescription Drug

Product NDC0121-4721

Product details

Brand name
Fluoxetine
Generic name
Fluoxetine Hydrochloride
Labeler
PAI Holdings, LLC dba PAI Pharma
Dosage form
Solution
Route
Oral
Marketing category
ANDA · ANDA076015
Marketed since
February 1, 2002
Listing expires
December 31, 2026
Pharmacologic class
Serotonin Reuptake Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Fluoxetine →

Package NDC codes (1)

Package NDCDescriptionSince
0121-4721-404 TRAY in 1 CASE (0121-4721-40) / 10 CUP, UNIT-DOSE in 1 TRAY / 5 mL in 1 CUP, UNIT-DOSE (0121-4721-05)Feb 1, 2002

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