Home > National Drug Code (NDC) > Ondansetron

Ondansetron - 55390-121-10 - (Ondansetron hydrochloride)

Alphabetical Index


Drug Information of Ondansetron

Product NDC: 55390-121
Proprietary Name: Ondansetron
Non Proprietary Name: Ondansetron hydrochloride
Active Ingredient(s): 2    mg/mL & nbsp;   Ondansetron hydrochloride
Administration Route(s): INTRAMUSCULAR; INTRAVENOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Ondansetron

Product NDC: 55390-121
Labeler Name: Bedford Laboratories
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076967
Marketing Category: ANDA
Start Marketing Date: 20061226

Package Information of Ondansetron

Package NDC: 55390-121-10
Package Description: 10 VIAL in 1 BOX (55390-121-10) > 2 mL in 1 VIAL

NDC Information of Ondansetron

NDC Code 55390-121-10
Proprietary Name Ondansetron
Package Description 10 VIAL in 1 BOX (55390-121-10) > 2 mL in 1 VIAL
Product NDC 55390-121
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Ondansetron hydrochloride
Dosage Form Name INJECTION, SOLUTION
Route Name INTRAMUSCULAR; INTRAVENOUS
Start Marketing Date 20061226
Marketing Category Name ANDA
Labeler Name Bedford Laboratories
Substance Name ONDANSETRON HYDROCHLORIDE
Strength Number 2
Strength Unit mg/mL
Pharmaceutical Classes Serotonin 3 Receptor Antagonists [MoA],Serotonin-3 Receptor Antagonist [EPC]

Complete Information of Ondansetron


General Information