NDC 71335-1357 – Ondansetron Hydrochloride

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

Human Prescription Drug

Product NDC71335-1357

Product details

Brand name
Ondansetron Hydrochloride
Generic name
Ondansetron Hydrochloride
Labeler
Bryant Ranch Prepack
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA078539
Marketed since
July 31, 2007
Listing expires
December 31, 2026
Pharmacologic class
Serotonin-3 Receptor Antagonist

Active ingredients

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

Package NDC codes (10)

Package NDCDescriptionSince
71335-1357-05 TABLET, FILM COATED in 1 BOTTLE (71335-1357-0)Apr 3, 2024
71335-1357-110 TABLET, FILM COATED in 1 BOTTLE (71335-1357-1)Oct 14, 2019
71335-1357-215 TABLET, FILM COATED in 1 BOTTLE (71335-1357-2)Jul 30, 2021
71335-1357-34 TABLET, FILM COATED in 1 BOTTLE (71335-1357-3)Apr 3, 2024
71335-1357-43 TABLET, FILM COATED in 1 BOTTLE (71335-1357-4)Apr 3, 2024
71335-1357-512 TABLET, FILM COATED in 1 BOTTLE (71335-1357-5)Sep 30, 2021
71335-1357-620 TABLET, FILM COATED in 1 BOTTLE (71335-1357-6)Sep 27, 2019
71335-1357-730 TABLET, FILM COATED in 1 BOTTLE (71335-1357-7)Oct 1, 2019
71335-1357-860 TABLET, FILM COATED in 1 BOTTLE (71335-1357-8)Jul 28, 2021
71335-1357-96 TABLET, FILM COATED in 1 BOTTLE (71335-1357-9)Feb 12, 2020

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