NDC 17856-0672 – Ondansetron

Ondansetron Hydrochloride 4 mg/5mL · Solution · Oral

Human Prescription Drug

Product NDC17856-0672

Product details

Brand name
Ondansetron
Generic name
Ondansetron Hydrochloride
Labeler
Atlantic Biologics Corp.
Dosage form
Solution
Route
Oral
Marketing category
ANDA · ANDA078776
Marketed since
November 28, 2007
Listing expires
December 31, 2026
Pharmacologic class
Serotonin-3 Receptor Antagonist

Active ingredients

Uses, dosage, side effects and warnings for Ondansetron →

Package NDC codes (4)

Package NDCDescriptionSince
17856-0672-160 SYRINGE in 1 CASE (17856-0672-1) / 2.5 mL in 1 SYRINGEOct 23, 2025
17856-0672-2120 SYRINGE in 1 CASE (17856-0672-2) / 2.5 mL in 1 SYRINGEOct 23, 2025
17856-0672-3120 SYRINGE in 1 CASE (17856-0672-3) / 2.5 mL in 1 SYRINGEOct 23, 2025
17856-0672-472 CUP, UNIT-DOSE in 1 CASE (17856-0672-4) / 5 mL in 1 CUP, UNIT-DOSEOct 23, 2025

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