NDC 17856-0691 – Ondansetron

Ondansetron Hydrochloride 4 mg/5mL · Solution · Oral

Human Prescription Drug

Product NDC17856-0691

Product details

Brand name
Ondansetron
Generic name
Ondansetron
Labeler
ATLANTIC BIOLOGICALS CORP.
Dosage form
Solution
Route
Oral
Marketing category
ANDA · ANDA091483
Marketed since
December 17, 2010
Listing expires
December 31, 2026
Pharmacologic class
Serotonin-3 Receptor Antagonist

Active ingredients

Uses, dosage, side effects and warnings for Ondansetron →

Package NDC codes (7)

Package NDCDescriptionSince
17856-0691-11.5 mL in 1 SYRINGE (17856-0691-1)Apr 17, 2024
17856-0691-22.5 mL in 1 SYRINGE, PLASTIC (17856-0691-2)Apr 17, 2024
17856-0691-42.5 mL in 1 SYRINGE, PLASTIC (17856-0691-4)Apr 17, 2024
17856-0691-55 mL in 1 CUP (17856-0691-5)Apr 17, 2024
17856-0691-6120 SYRINGE in 1 BOX, UNIT-DOSE (17856-0691-6) / 1.25 mL in 1 SYRINGEApr 17, 2024
17856-0691-748 SYRINGE in 1 BOX, UNIT-DOSE (17856-0691-7) / 1.9 mL in 1 SYRINGEApr 17, 2024
17856-0691-860 SYRINGE in 1 BOX, UNIT-DOSE (17856-0691-8) / 2.5 mL in 1 SYRINGEApr 17, 2024

Other Ondansetron products