Home > National Drug Code (NDC) > Ondansetron Hydrochloride

Ondansetron Hydrochloride - 23155-196-41 - (Ondansetron Hydrochloride)

Alphabetical Index


Drug Information of Ondansetron Hydrochloride

Product NDC: 23155-196
Proprietary Name: Ondansetron Hydrochloride
Non Proprietary Name: Ondansetron Hydrochloride
Active Ingredient(s): 2    mg/mL & nbsp;   Ondansetron Hydrochloride
Administration Route(s): INTRAVENOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Ondansetron Hydrochloride

Product NDC: 23155-196
Labeler Name: Heritage Pharmaceuticals Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078945
Marketing Category: ANDA
Start Marketing Date: 20130118

Package Information of Ondansetron Hydrochloride

Package NDC: 23155-196-41
Package Description: 5 VIAL in 1 CARTON (23155-196-41) > 2 mL in 1 VIAL (23155-196-31)

NDC Information of Ondansetron Hydrochloride

NDC Code 23155-196-41
Proprietary Name Ondansetron Hydrochloride
Package Description 5 VIAL in 1 CARTON (23155-196-41) > 2 mL in 1 VIAL (23155-196-31)
Product NDC 23155-196
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Ondansetron Hydrochloride
Dosage Form Name INJECTION, SOLUTION
Route Name INTRAVENOUS
Start Marketing Date 20130118
Marketing Category Name ANDA
Labeler Name Heritage Pharmaceuticals Inc.
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 Hydrochloride


General Information