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Ondansetron - 68462-158-11 - (Ondansetron)

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Drug Information of Ondansetron

Product NDC: 68462-158
Proprietary Name: Ondansetron
Non Proprietary Name: Ondansetron
Active Ingredient(s): 8    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: 68462-158
Labeler Name: Glenmark Generics Inc., USA
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078152
Marketing Category: ANDA
Start Marketing Date: 20070627

Package Information of Ondansetron

Package NDC: 68462-158-11
Package Description: 10 TABLET, ORALLY DISINTEGRATING in 1 BOX, UNIT-DOSE (68462-158-11)

NDC Information of Ondansetron

NDC Code 68462-158-11
Proprietary Name Ondansetron
Package Description 10 TABLET, ORALLY DISINTEGRATING in 1 BOX, UNIT-DOSE (68462-158-11)
Product NDC 68462-158
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 Glenmark Generics Inc., USA
Substance Name ONDANSETRON
Strength Number 8
Strength Unit mg/1
Pharmaceutical Classes Serotonin 3 Receptor Antagonists [MoA],Serotonin-3 Receptor Antagonist [EPC]

Complete Information of Ondansetron


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