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Ondansetron - 0781-5239-80 - (Ondansetron)

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Drug Information of Ondansetron

Product NDC: 0781-5239
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: 0781-5239
Labeler Name: Sandoz Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078050
Marketing Category: ANDA
Start Marketing Date: 20070813

Package Information of Ondansetron

Package NDC: 0781-5239-80
Package Description: 1 BLISTER PACK in 1 CARTON (0781-5239-80) > 10 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK (0781-5239-06)

NDC Information of Ondansetron

NDC Code 0781-5239-80
Proprietary Name Ondansetron
Package Description 1 BLISTER PACK in 1 CARTON (0781-5239-80) > 10 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK (0781-5239-06)
Product NDC 0781-5239
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Ondansetron
Dosage Form Name TABLET, ORALLY DISINTEGRATING
Route Name ORAL
Start Marketing Date 20070813
Marketing Category Name ANDA
Labeler Name Sandoz Inc
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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