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Ondansetron Hydrochloride - 51672-4109-6 - (Ondansetron Hydrochloride)

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Drug Information of Ondansetron Hydrochloride

Product NDC: 51672-4109
Proprietary Name: Ondansetron Hydrochloride
Non Proprietary Name: Ondansetron Hydrochloride
Active Ingredient(s): 8    mg/1 & nbsp;   Ondansetron Hydrochloride
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Ondansetron Hydrochloride

Product NDC: 51672-4109
Labeler Name: Taro Pharmaceuticals U.S.A., Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077729
Marketing Category: ANDA
Start Marketing Date: 20110328

Package Information of Ondansetron Hydrochloride

Package NDC: 51672-4109-6
Package Description: 30 TABLET, FILM COATED in 1 BOTTLE (51672-4109-6)

NDC Information of Ondansetron Hydrochloride

NDC Code 51672-4109-6
Proprietary Name Ondansetron Hydrochloride
Package Description 30 TABLET, FILM COATED in 1 BOTTLE (51672-4109-6)
Product NDC 51672-4109
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Ondansetron Hydrochloride
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20110328
Marketing Category Name ANDA
Labeler Name Taro Pharmaceuticals U.S.A., Inc.
Substance Name ONDANSETRON HYDROCHLORIDE
Strength Number 8
Strength Unit mg/1
Pharmaceutical Classes Serotonin 3 Receptor Antagonists [MoA],Serotonin-3 Receptor Antagonist [EPC]

Complete Information of Ondansetron Hydrochloride


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