NDC 72162-2365 – Ondansetron Hydrochloride

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

Human Prescription Drug

Product NDC72162-2365

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 (1)

Package NDCDescriptionSince
72162-2365-5500 TABLET, FILM COATED in 1 BOTTLE (72162-2365-5)Jul 16, 2024

Other Ondansetron hydrochloride products