Search by Drug Name or NDC

NDC 55154-7879-00 ondansetron hydrochloride 8 mg/1 Details

ondansetron hydrochloride 8 mg/1

ondansetron hydrochloride is a ORAL TABLET, FILM COATED in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Cardinal Health 107, LLC. The primary component is ONDANSETRON HYDROCHLORIDE.

MedlinePlus Drug Summary

Ondansetron is used to prevent nausea and vomiting caused by cancer chemotherapy, radiation therapy, and surgery. Ondansetron is in a class of medications called serotonin 5-HT3 receptor antagonists. It works by blocking the action of serotonin, a natural substance that may cause nausea and vomiting.

Related Packages: 55154-7879-00
Last Updated: 04/21/2024
MedLinePlus Full Drug Details: Ondansetron

Product Information

NDC	55154-7879
Product ID	55154-7879_4db69d8a-6318-46d3-8617-042fb716e1ec
Associated GPIs
GCN Sequence Number	n/a
GCN Sequence Number Description	n/a
HIC3	n/a
HIC3 Description	n/a
GCN	n/a
HICL Sequence Number	n/a
HICL Sequence Number Description	n/a
Brand/Generic	n/a
Proprietary Name	ondansetron hydrochloride
Proprietary Name Suffix	n/a
Non-Proprietary Name	ondansetron hydrochloride
Product Type	HUMAN PRESCRIPTION DRUG
Dosage Form	TABLET, FILM COATED
Route	ORAL
Active Ingredient Strength	8
Active Ingredient Units	mg/1
Substance Name	ONDANSETRON HYDROCHLORIDE
Labeler Name	Cardinal Health 107, LLC
Pharmaceutical Class	Serotonin 3 Receptor Antagonists [MoA], Serotonin-3 Receptor Antagonist [EPC]
DEA Schedule	n/a
Marketing Category	ANDA
Application Number	ANDA076183
Listing Certified Through	2024-12-31

Package

NDC 55154-7879-00 (55154787900)

Pricing Information	N/A
NDC Package Code	55154-7879-0
Billing NDC	55154787900
Package	10 BLISTER PACK in 1 BAG (55154-7879-0) / 1 TABLET, FILM COATED in 1 BLISTER PACK
Marketing Start Date	2006-12-26
NDC Exclude Flag	N