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Ondansetron - 55154-5431-0 - (Ondansetron)

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Drug Information of Ondansetron

Product NDC: 55154-5431
Proprietary Name: Ondansetron
Non Proprietary Name: Ondansetron
Active Ingredient(s): 4    mg/1 & nbsp;   Ondansetron
Administration Route(s): ORAL
Dosage Form(s): TABLET, ORALLY DISINTEGRATING
Coding System: National Drug Codes(NDC)

Labeler Information of Ondansetron

Product NDC: 55154-5431
Labeler Name: Cardinal Health
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078050
Marketing Category: ANDA
Start Marketing Date: 20070831

Package Information of Ondansetron

Package NDC: 55154-5431-0
Package Description: 10 BLISTER PACK in 1 BAG (55154-5431-0) > 1 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK

NDC Information of Ondansetron

NDC Code 55154-5431-0
Proprietary Name Ondansetron
Package Description 10 BLISTER PACK in 1 BAG (55154-5431-0) > 1 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK
Product NDC 55154-5431
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Ondansetron
Dosage Form Name TABLET, ORALLY DISINTEGRATING
Route Name ORAL
Start Marketing Date 20070831
Marketing Category Name ANDA
Labeler Name Cardinal Health
Substance Name ONDANSETRON
Strength Number 4
Strength Unit mg/1
Pharmaceutical Classes Serotonin 3 Receptor Antagonists [MoA],Serotonin-3 Receptor Antagonist [EPC]

Complete Information of Ondansetron


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