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Ondansetron Hydrochloride - 0781-1681-31 - (Ondansetron Hydrochloride)

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Drug Information of Ondansetron Hydrochloride

Product NDC: 0781-1681
Proprietary Name: Ondansetron Hydrochloride
Non Proprietary Name: Ondansetron Hydrochloride
Active Ingredient(s): 8    mg/1 & nbsp;   Ondansetron Hydrochloride
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Ondansetron Hydrochloride

Product NDC: 0781-1681
Labeler Name: Sandoz Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077517
Marketing Category: ANDA
Start Marketing Date: 20070625

Package Information of Ondansetron Hydrochloride

Package NDC: 0781-1681-31
Package Description: 30 TABLET, FILM COATED in 1 BOTTLE (0781-1681-31)

NDC Information of Ondansetron Hydrochloride

NDC Code 0781-1681-31
Proprietary Name Ondansetron Hydrochloride
Package Description 30 TABLET, FILM COATED in 1 BOTTLE (0781-1681-31)
Product NDC 0781-1681
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Ondansetron Hydrochloride
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20070625
Marketing Category Name ANDA
Labeler Name Sandoz Inc
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 Hydrochloride


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