NDC 69339-172 – Ondansetron

Ondansetron Hydrochloride 8 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC69339-172

Product details

Brand name
Ondansetron
Generic name
Ondansetron
Labeler
Natco Pharma USA LLC
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA077851
Marketed since
October 24, 2022
Listing expires
December 31, 2026
Pharmacologic class
Serotonin-3 Receptor Antagonist

Active ingredients

Uses, dosage, side effects and warnings for Ondansetron →

Package NDC codes (3)

Package NDCDescriptionSince
69339-172-01100 TABLET in 1 BOTTLE (69339-172-01)Jun 27, 2025
69339-172-0330 TABLET in 1 BOTTLE (69339-172-03)Oct 24, 2022
69339-172-05500 TABLET in 1 BOTTLE (69339-172-05)Jun 27, 2025

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