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Ondansetron - 0703-7226-03 - (Ondansetron)

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Drug Information of Ondansetron

Product NDC: 0703-7226
Proprietary Name: Ondansetron
Non Proprietary Name: Ondansetron
Active Ingredient(s): 2    mg/mL & nbsp;   Ondansetron
Administration Route(s): INTRAMUSCULAR; INTRAVENOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Ondansetron

Product NDC: 0703-7226
Labeler Name: Teva Parenteral Medicines, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076876
Marketing Category: ANDA
Start Marketing Date: 20061122

Package Information of Ondansetron

Package NDC: 0703-7226-03
Package Description: 10 VIAL, MULTI-DOSE in 1 CARTON (0703-7226-03) > 20 mL in 1 VIAL, MULTI-DOSE

NDC Information of Ondansetron

NDC Code 0703-7226-03
Proprietary Name Ondansetron
Package Description 10 VIAL, MULTI-DOSE in 1 CARTON (0703-7226-03) > 20 mL in 1 VIAL, MULTI-DOSE
Product NDC 0703-7226
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Ondansetron
Dosage Form Name INJECTION, SOLUTION
Route Name INTRAMUSCULAR; INTRAVENOUS
Start Marketing Date 20061122
Marketing Category Name ANDA
Labeler Name Teva Parenteral Medicines, 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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