NDC 0121-4882 – Ondansetron

Ondansetron Hydrochloride 4 mg/5mL · Solution · Oral

Human Prescription Drug

Product NDC0121-4882

Product details

Brand name
Ondansetron
Generic name
Ondansetron
Labeler
PAI Holdings, LLC dba PAI Pharma
Dosage form
Solution
Route
Oral
Marketing category
ANDA · ANDA078127
Marketed since
June 9, 2026
Listing expires
December 31, 2027
Pharmacologic class
Serotonin-3 Receptor Antagonist

Active ingredients

Uses, dosage, side effects and warnings for Ondansetron →

Package NDC codes (1)

Package NDCDescriptionSince
0121-4882-943 TRAY in 1 CASE (0121-4882-94) / 10 CUP in 1 TRAY / 5 mL in 1 CUP (0121-4882-05)Jun 9, 2026

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