NDC 85766-006 – Ondansetron Hydrochloride

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

Human Prescription Drug

Product NDC85766-006

Product details

Brand name
Ondansetron Hydrochloride
Generic name
Ondansetron Hydrochloride
Labeler
Sportpharm LLC
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA078539
Marketed since
July 31, 2007
Listing expires
December 31, 2027
Pharmacologic class
Serotonin-3 Receptor Antagonist

Active ingredients

Uses, dosage, side effects and warnings for Ondansetron hydrochloride →

Package NDC codes (10)

Package NDCDescriptionSince
85766-006-001000 TABLET, FILM COATED in 1 BOTTLE (85766-006-00)Jun 19, 2025
85766-006-033 TABLET, FILM COATED in 1 BOTTLE (85766-006-03)Jun 19, 2025
85766-006-05500 TABLET, FILM COATED in 1 BOTTLE (85766-006-05)Jun 19, 2025
85766-006-066 TABLET, FILM COATED in 1 BOTTLE (85766-006-06)Jun 19, 2025
85766-006-088 TABLET, FILM COATED in 1 BOTTLE (85766-006-08)May 4, 2026
85766-006-1010 TABLET, FILM COATED in 1 BOTTLE (85766-006-10)Jun 19, 2025
85766-006-2424 TABLET, FILM COATED in 1 BOTTLE (85766-006-24)Oct 1, 2025
85766-006-3030 TABLET, FILM COATED in 1 BOTTLE (85766-006-30)Jun 19, 2025
85766-006-6060 TABLET, FILM COATED in 1 BOTTLE (85766-006-60)Jun 19, 2025
85766-006-9090 TABLET, FILM COATED in 1 BOTTLE (85766-006-90)Jun 19, 2025

Other Ondansetron hydrochloride products