NDC 42708-179 – Ondansetron Hydrochloride

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

Human Prescription Drug

Product NDC42708-179

Product details

Brand name
Ondansetron Hydrochloride
Generic name
Ondansetron Hydrochloride
Labeler
QPharma, Inc.
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 (1)

Package NDCDescriptionSince
42708-179-05 sample5 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (42708-179-05)May 19, 2023

Other Ondansetron hydrochloride products