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Ondansetron - 68462-106-33 - (Ondansetron)

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Drug Information of Ondansetron

Product NDC: 68462-106
Proprietary Name: Ondansetron
Non Proprietary Name: Ondansetron
Active Ingredient(s): 8    mg/1 & nbsp;   Ondansetron
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Ondansetron

Product NDC: 68462-106
Labeler Name: Glenmark Generics Inc., USA
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077535
Marketing Category: ANDA
Start Marketing Date: 20070625

Package Information of Ondansetron

Package NDC: 68462-106-33
Package Description: 1 BLISTER PACK in 1 CARTON (68462-106-33) > 3 TABLET, FILM COATED in 1 BLISTER PACK

NDC Information of Ondansetron

NDC Code 68462-106-33
Proprietary Name Ondansetron
Package Description 1 BLISTER PACK in 1 CARTON (68462-106-33) > 3 TABLET, FILM COATED in 1 BLISTER PACK
Product NDC 68462-106
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Ondansetron
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20070625
Marketing Category Name ANDA
Labeler Name Glenmark Generics Inc., USA
Substance Name ONDANSETRON HYDROCHLORIDE
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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