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Ondansetron - 51672-4091-3 - (ondansetron hydrochloride)

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Drug Information of Ondansetron

Product NDC: 51672-4091
Proprietary Name: Ondansetron
Non Proprietary Name: ondansetron hydrochloride
Active Ingredient(s): 4    mg/5mL & nbsp;   ondansetron hydrochloride
Administration Route(s): ORAL
Dosage Form(s): SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Ondansetron

Product NDC: 51672-4091
Labeler Name: Taro Pharmaceuticals U.S.A., Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077009
Marketing Category: ANDA
Start Marketing Date: 20071130

Package Information of Ondansetron

Package NDC: 51672-4091-3
Package Description: 1 BOTTLE in 1 CARTON (51672-4091-3) > 50 mL in 1 BOTTLE

NDC Information of Ondansetron

NDC Code 51672-4091-3
Proprietary Name Ondansetron
Package Description 1 BOTTLE in 1 CARTON (51672-4091-3) > 50 mL in 1 BOTTLE
Product NDC 51672-4091
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name ondansetron hydrochloride
Dosage Form Name SOLUTION
Route Name ORAL
Start Marketing Date 20071130
Marketing Category Name ANDA
Labeler Name Taro Pharmaceuticals U.S.A., Inc.
Substance Name ONDANSETRON HYDROCHLORIDE
Strength Number 4
Strength Unit mg/5mL
Pharmaceutical Classes Serotonin 3 Receptor Antagonists [MoA],Serotonin-3 Receptor Antagonist [EPC]

Complete Information of Ondansetron


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