NDC 71335-1855 – Ondansetron Hydrochloride

Ondansetron Hydrochloride 4 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC71335-1855

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
71335-1855-060 TABLET, FILM COATED in 1 BOTTLE (71335-1855-0)Dec 21, 2021
71335-1855-110 TABLET, FILM COATED in 1 BOTTLE (71335-1855-1)Dec 21, 2021
71335-1855-23 TABLET, FILM COATED in 1 BOTTLE (71335-1855-2)Dec 21, 2021
71335-1855-330 TABLET, FILM COATED in 1 BOTTLE (71335-1855-3)Dec 21, 2021
71335-1855-415 TABLET, FILM COATED in 1 BOTTLE (71335-1855-4)Dec 21, 2021
71335-1855-56 TABLET, FILM COATED in 1 BOTTLE (71335-1855-5)Dec 21, 2021
71335-1855-64 TABLET, FILM COATED in 1 BOTTLE (71335-1855-6)Dec 21, 2021
71335-1855-790 TABLET, FILM COATED in 1 BOTTLE (71335-1855-7)Dec 21, 2021
71335-1855-812 TABLET, FILM COATED in 1 BOTTLE (71335-1855-8)Dec 21, 2021
71335-1855-920 TABLET, FILM COATED in 1 BOTTLE (71335-1855-9)Dec 21, 2021

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