NDC 71335-0132 – Ondansetron

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

Human Prescription Drug

Product NDC71335-0132

Product details

Brand name
Ondansetron
Generic name
Ondansetron
Labeler
Bryant Ranch Prepack
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA077851
Marketed since
July 27, 2007
Listing expires
December 31, 2026
Pharmacologic class
Serotonin-3 Receptor Antagonist

Active ingredients

Uses, dosage, side effects and warnings for Ondansetron →

Package NDC codes (10)

Package NDCDescriptionSince
71335-0132-060 TABLET, FILM COATED in 1 BOTTLE (71335-0132-0)Apr 3, 2014
71335-0132-110 TABLET, FILM COATED in 1 BOTTLE (71335-0132-1)Apr 3, 2014
71335-0132-23 TABLET, FILM COATED in 1 BOTTLE (71335-0132-2)Apr 3, 2014
71335-0132-330 TABLET, FILM COATED in 1 BOTTLE (71335-0132-3)Apr 3, 2014
71335-0132-415 TABLET, FILM COATED in 1 BOTTLE (71335-0132-4)Apr 3, 2014
71335-0132-56 TABLET, FILM COATED in 1 BOTTLE (71335-0132-5)Apr 3, 2014
71335-0132-64 TABLET, FILM COATED in 1 BOTTLE (71335-0132-6)Apr 3, 2014
71335-0132-790 TABLET, FILM COATED in 1 BOTTLE (71335-0132-7)Apr 3, 2014
71335-0132-812 TABLET, FILM COATED in 1 BOTTLE (71335-0132-8)Apr 3, 2014
71335-0132-920 TABLET, FILM COATED in 1 BOTTLE (71335-0132-9)Apr 3, 2014

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