Home > National Drug Code (NDC) > ONDANSETRON HYDROCHLORIDE

ONDANSETRON HYDROCHLORIDE - 63629-4093-4 - (ONDANSETRON HYDROCHLORIDE)

Alphabetical Index


Drug Information of ONDANSETRON HYDROCHLORIDE

Product NDC: 63629-4093
Proprietary Name: ONDANSETRON HYDROCHLORIDE
Non Proprietary Name: ONDANSETRON HYDROCHLORIDE
Active Ingredient(s): 8    mg/1 & nbsp;   ONDANSETRON HYDROCHLORIDE
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of ONDANSETRON HYDROCHLORIDE

Product NDC: 63629-4093
Labeler Name: Bryant Ranch Prepack
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077050
Marketing Category: ANDA
Start Marketing Date: 20070625

Package Information of ONDANSETRON HYDROCHLORIDE

Package NDC: 63629-4093-4
Package Description: 3 TABLET, FILM COATED in 1 BOTTLE (63629-4093-4)

NDC Information of ONDANSETRON HYDROCHLORIDE

NDC Code 63629-4093-4
Proprietary Name ONDANSETRON HYDROCHLORIDE
Package Description 3 TABLET, FILM COATED in 1 BOTTLE (63629-4093-4)
Product NDC 63629-4093
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name ONDANSETRON HYDROCHLORIDE
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20070625
Marketing Category Name ANDA
Labeler Name Bryant Ranch Prepack
Substance Name ONDANSETRON HYDROCHLORIDE
Strength Number 8
Strength Unit mg/1
Pharmaceutical Classes Serotonin 3 Receptor Antagonists [MoA],Serotonin-3 Receptor Antagonist [EPC]

Complete Information of ONDANSETRON HYDROCHLORIDE


General Information