NDC 76420-915 – Ondansetron Hydrochloride

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

Human Prescription Drug

Product NDC76420-915

Product details

Brand name
Ondansetron Hydrochloride
Generic name
Ondansetron Hydrochloride
Labeler
Asclemed USA, 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 (9)

Package NDCDescriptionSince
76420-915-001000 TABLET, FILM COATED in 1 BOTTLE (76420-915-00)Jan 28, 2025
76420-915-033 TABLET, FILM COATED in 1 BOTTLE (76420-915-03)Jan 28, 2025
76420-915-05500 TABLET, FILM COATED in 1 BOTTLE (76420-915-05)Jan 28, 2025
76420-915-1010 TABLET, FILM COATED in 1 BOTTLE (76420-915-10)Jan 28, 2025
76420-915-1110 BLISTER PACK in 1 CARTON (76420-915-11) / 10 TABLET, FILM COATED in 1 BLISTER PACKJan 28, 2025
76420-915-3030 TABLET, FILM COATED in 1 BOTTLE (76420-915-30)Jan 28, 2025
76420-915-331 BLISTER PACK in 1 CARTON (76420-915-33) / 3 TABLET, FILM COATED in 1 BLISTER PACKJan 28, 2025
76420-915-6060 TABLET, FILM COATED in 1 BOTTLE (76420-915-60)Jan 28, 2025
76420-915-9090 TABLET, FILM COATED in 1 BOTTLE (76420-915-90)Jan 28, 2025

Other Ondansetron hydrochloride products