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Ondansetron - 54868-5888-0 - (Ondansetron Hydrochloride)

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Drug Information of Ondansetron

Product NDC: 54868-5888
Proprietary Name: Ondansetron
Non Proprietary Name: Ondansetron Hydrochloride
Active Ingredient(s): 2    mg/mL & nbsp;   Ondansetron Hydrochloride
Administration Route(s): INTRAVENOUS
Dosage Form(s): INJECTION
Coding System: National Drug Codes(NDC)

Labeler Information of Ondansetron

Product NDC: 54868-5888
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076781
Marketing Category: ANDA
Start Marketing Date: 20080508

Package Information of Ondansetron

Package NDC: 54868-5888-0
Package Description: 5 VIAL in 1 CARTON (54868-5888-0) > 2 mL in 1 VIAL

NDC Information of Ondansetron

NDC Code 54868-5888-0
Proprietary Name Ondansetron
Package Description 5 VIAL in 1 CARTON (54868-5888-0) > 2 mL in 1 VIAL
Product NDC 54868-5888
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Ondansetron Hydrochloride
Dosage Form Name INJECTION
Route Name INTRAVENOUS
Start Marketing Date 20080508
Marketing Category Name ANDA
Labeler Name Physicians Total Care, 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


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