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Ondansetron - 65862-390-10 - (Ondansetron)

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Drug Information of Ondansetron

Product NDC: 65862-390
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: 65862-390
Labeler Name: Aurobindo Pharma Limited
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA090469
Marketing Category: ANDA
Start Marketing Date: 20100412

Package Information of Ondansetron

Package NDC: 65862-390-10
Package Description: 3 BLISTER PACK in 1 CARTON (65862-390-10) > 10 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK

NDC Information of Ondansetron

NDC Code 65862-390-10
Proprietary Name Ondansetron
Package Description 3 BLISTER PACK in 1 CARTON (65862-390-10) > 10 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK
Product NDC 65862-390
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Ondansetron
Dosage Form Name TABLET, ORALLY DISINTEGRATING
Route Name ORAL
Start Marketing Date 20100412
Marketing Category Name ANDA
Labeler Name Aurobindo Pharma Limited
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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