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Ondansetron Hydrochloride - 60505-1312-4 - (ondansetron hydrochloride)

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Drug Information of Ondansetron Hydrochloride

Product NDC: 60505-1312
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
Coding System: National Drug Codes(NDC)

Labeler Information of Ondansetron Hydrochloride

Product NDC: 60505-1312
Labeler Name: Apotex Corp.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077306
Marketing Category: ANDA
Start Marketing Date: 20081111

Package Information of Ondansetron Hydrochloride

Package NDC: 60505-1312-4
Package Description: 1 BLISTER PACK in 1 CARTON (60505-1312-4) > 3 TABLET in 1 BLISTER PACK

NDC Information of Ondansetron Hydrochloride

NDC Code 60505-1312-4
Proprietary Name Ondansetron Hydrochloride
Package Description 1 BLISTER PACK in 1 CARTON (60505-1312-4) > 3 TABLET in 1 BLISTER PACK
Product NDC 60505-1312
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name ondansetron hydrochloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20081111
Marketing Category Name ANDA
Labeler Name Apotex Corp.
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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