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NDC 68462-0105-33 Ondansetron 4 mg/1 Details

Ondansetron 4 mg/1

Ondansetron is a ORAL TABLET, FILM COATED in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Glenmark Pharmaceuticals Inc., USA. 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: 68462-0105-33
Last Updated: 12/01/2022
MedLinePlus Full Drug Details: Ondansetron

Product Information

NDC	68462-0105
Product ID	68462-105_ca1eb3c3-a781-4b63-bbdb-e0d2e3c9c8c5
Associated GPIs	50250065050310
GCN Sequence Number	016392
GCN Sequence Number Description	ondansetron HCl TABLET 4 MG ORAL
HIC3	H6J
HIC3 Description	ANTIEMETIC/ANTIVERTIGO AGENTS
GCN	20041
HICL Sequence Number	006055
HICL Sequence Number Description	ONDANSETRON HCL
Brand/Generic	Generic
Proprietary Name	Ondansetron
Proprietary Name Suffix	n/a
Non-Proprietary Name	Ondansetron
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	Glenmark Pharmaceuticals Inc., USA
Pharmaceutical Class	Serotonin 3 Receptor Antagonists [MoA], Serotonin-3 Receptor Antagonist [EPC]
DEA Schedule	n/a
Marketing Category	ANDA
Application Number	ANDA077535
Listing Certified Through	2025-12-31

Package

NDC 68462-0105-33 (68462010533)

Pricing Information	N/A
NDC Package Code	68462-105-33
Billing NDC	68462010533
Package	1 BLISTER PACK in 1 CARTON (68462-105-33) / 3 TABLET, FILM COATED in 1 BLISTER PACK
Marketing Start Date	2007-06-25
NDC Exclude Flag	N