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NDC 70934-0264-10 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 Denton Pharma, Inc. DBA Northwind Pharmaceuticals. 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: 70934-0264-10
Last Updated: 12/01/2022
MedLinePlus Full Drug Details: Ondansetron

Product Information

NDC	70934-0264
Product ID	70934-264_d73449b9-4962-5122-e053-2995a90abc9d
Associated GPIs	50250065050320
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	Denton Pharma, Inc. DBA Northwind Pharmaceuticals
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	n/a

Package

NDC 70934-0264-10 (70934026410)

Pricing Information	N/A
NDC Package Code	70934-264-10
Billing NDC	70934026410
Package	10 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70934-264-10)
Marketing Start Date	2020-03-09
NDC Exclude Flag	N