NDC 50090-6342 – Ondansetron Hydrochloride

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

Human Prescription Drug

Product NDC50090-6342

Product details

Brand name
Ondansetron Hydrochloride
Generic name
Ondansetron Hydrochloride
Labeler
A-S Medication Solutions
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 (5)

Package NDCDescriptionSince
50090-6342-010 TABLET, FILM COATED in 1 BOTTLE (50090-6342-0)Jan 23, 2023
50090-6342-16 TABLET, FILM COATED in 1 BOTTLE (50090-6342-1)Jan 23, 2023
50090-6342-220 TABLET, FILM COATED in 1 BOTTLE (50090-6342-2)Jan 23, 2023
50090-6342-43 TABLET, FILM COATED in 1 BOTTLE (50090-6342-4)Jan 23, 2023
50090-6342-512 TABLET, FILM COATED in 1 BOTTLE (50090-6342-5)Jan 23, 2023

Other Ondansetron hydrochloride products