NDC 76420-916 – Ondansetron Hydrochloride

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

Human Prescription Drug

Product NDC76420-916

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
76420-916-001000 TABLET, FILM COATED in 1 BOTTLE (76420-916-00)Jan 28, 2025
76420-916-033 TABLET, FILM COATED in 1 BOTTLE (76420-916-03)Jan 28, 2025
76420-916-05500 TABLET, FILM COATED in 1 BOTTLE (76420-916-05)Jan 28, 2025
76420-916-1010 TABLET, FILM COATED in 1 BOTTLE (76420-916-10)Jan 28, 2025
76420-916-1110 BLISTER PACK in 1 CARTON (76420-916-11) / 10 TABLET, FILM COATED in 1 BLISTER PACKJan 28, 2025
76420-916-3030 TABLET, FILM COATED in 1 BOTTLE (76420-916-30)Jan 28, 2025
76420-916-331 BLISTER PACK in 1 CARTON (76420-916-33) / 3 TABLET, FILM COATED in 1 BLISTER PACKJan 28, 2025
76420-916-6060 TABLET, FILM COATED in 1 BOTTLE (76420-916-60)Jan 28, 2025
76420-916-9090 TABLET, FILM COATED in 1 BOTTLE (76420-916-90)Jan 28, 2025

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