Search by Drug Name or NDC

NDC 68788-9368-03 Ondansetron Hydrochloride 4 mg/1 Details

Ondansetron Hydrochloride 4 mg/1

Ondansetron Hydrochloride is a ORAL TABLET, FILM COATED in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Preferred Pharmaceuticals, Inc.. 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: 68788-9368-03
Last Updated: 12/01/2022
MedLinePlus Full Drug Details: Ondansetron

Product Information

NDC	68788-9368
Product ID	68788-9368_d4ce06ae-a386-41a4-828c-72391dda6f7d
Associated GPIs	50250065050310
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	4
Active Ingredient Units	mg/1
Substance Name	ONDANSETRON HYDROCHLORIDE
Labeler Name	Preferred Pharmaceuticals, Inc.
Pharmaceutical Class	Serotonin 3 Receptor Antagonists [MoA], Serotonin-3 Receptor Antagonist [EPC]
DEA Schedule	n/a
Marketing Category	ANDA
Application Number	ANDA078539
Listing Certified Through	2024-12-31

Package

NDC 68788-9368-03 (68788936803)

Pricing Information	N/A
NDC Package Code	68788-9368-3
Billing NDC	68788936803
Package	30 TABLET, FILM COATED in 1 BOTTLE (68788-9368-3)
Marketing Start Date	2012-06-12
NDC Exclude Flag	N