NDC 85766-053 – Ondansetron Hydrochloride

Ondansetron Hydrochloride 8 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC85766-053

Product details

Brand name
Ondansetron Hydrochloride
Generic name
Ondansetron Hydrochloride
Labeler
Sportpharm LLC
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA078539
Marketed since
July 31, 2007
Listing expires
December 31, 2027
Pharmacologic class
Serotonin-3 Receptor Antagonist

Active ingredients

Uses, dosage, side effects and warnings for Ondansetron hydrochloride →

Package NDC codes (8)

Package NDCDescriptionSince
85766-053-055 TABLET, FILM COATED in 1 BOTTLE (85766-053-05)Oct 1, 2025
85766-053-1010 TABLET, FILM COATED in 1 BOTTLE (85766-053-10)Oct 1, 2025
85766-053-1414 TABLET, FILM COATED in 1 BOTTLE (85766-053-14)Oct 1, 2025
85766-053-2020 TABLET, FILM COATED in 1 BOTTLE (85766-053-20)Oct 1, 2025
85766-053-2424 TABLET, FILM COATED in 1 BOTTLE (85766-053-24)Oct 1, 2025
85766-053-3030 TABLET, FILM COATED in 1 BOTTLE (85766-053-30)Oct 1, 2025
85766-053-6060 TABLET, FILM COATED in 1 BOTTLE (85766-053-60)Oct 1, 2025
85766-053-9090 TABLET, FILM COATED in 1 BOTTLE (85766-053-90)Oct 1, 2025

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