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NDC 55700-0631-06 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 Quality Care Products 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: 55700-0631-06
Last Updated: 11/30/2022
MedLinePlus Full Drug Details: Ondansetron

Product Information

NDC	55700-0631
Product ID	55700-631_8fc12712-574c-4eb5-9859-174e2c34d3d2
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 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	Quality Care Products LLC
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 55700-0631-06 (55700063106)

Pricing Information	N/A
NDC Package Code	55700-631-06
Billing NDC	55700063106
Package	6 TABLET, FILM COATED in 1 BOTTLE (55700-631-06)
Marketing Start Date	2018-05-25
NDC Exclude Flag	N