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Ondansetron - 52125-568-02 - (Ondansetron)

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Drug Information of Ondansetron

Product NDC: 52125-568
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: 52125-568
Labeler Name: REMEDYREPACK INC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078152
Marketing Category: ANDA
Start Marketing Date: 20130610

Package Information of Ondansetron

Package NDC: 52125-568-02
Package Description: 30 TABLET, ORALLY DISINTEGRATING in 1 BOX, UNIT-DOSE (52125-568-02)

NDC Information of Ondansetron

NDC Code 52125-568-02
Proprietary Name Ondansetron
Package Description 30 TABLET, ORALLY DISINTEGRATING in 1 BOX, UNIT-DOSE (52125-568-02)
Product NDC 52125-568
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Ondansetron
Dosage Form Name TABLET, ORALLY DISINTEGRATING
Route Name ORAL
Start Marketing Date 20130610
Marketing Category Name ANDA
Labeler Name REMEDYREPACK INC.
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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