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Ondansetron Hydrochloride - 63629-4014-2 - (Ondansetron)

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Drug Information of Ondansetron Hydrochloride

Product NDC: 63629-4014
Proprietary Name: Ondansetron Hydrochloride
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 Hydrochloride

Product NDC: 63629-4014
Labeler Name: Bryant Ranch Prepack
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078152
Marketing Category: ANDA
Start Marketing Date: 20070627

Package Information of Ondansetron Hydrochloride

Package NDC: 63629-4014-2
Package Description: 15 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE (63629-4014-2)

NDC Information of Ondansetron Hydrochloride

NDC Code 63629-4014-2
Proprietary Name Ondansetron Hydrochloride
Package Description 15 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE (63629-4014-2)
Product NDC 63629-4014
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Ondansetron
Dosage Form Name TABLET, ORALLY DISINTEGRATING
Route Name ORAL
Start Marketing Date 20070627
Marketing Category Name ANDA
Labeler Name Bryant Ranch Prepack
Substance Name ONDANSETRON HYDROCHLORIDE
Strength Number 4
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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