NDC 0121-0882 – Ondansetron

Ondansetron Hydrochloride 4 mg/5mL · Solution · Oral

Human Prescription Drug

Product NDC0121-0882

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
April 20, 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
0121-0882-5150 mL in 1 BOTTLE, PLASTIC (0121-0882-51)Apr 20, 2026

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