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Ondansetron - 0143-2423-01 - (Ondansetron hydrochloride)

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Drug Information of Ondansetron

Product NDC: 0143-2423
Proprietary Name: Ondansetron
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

Product NDC: 0143-2423
Labeler Name: West-ward Pharmaceutical Corp
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077545
Marketing Category: ANDA
Start Marketing Date: 20080101

Package Information of Ondansetron

Package NDC: 0143-2423-01
Package Description: 100 TABLET in 1 BOTTLE, GLASS (0143-2423-01)

NDC Information of Ondansetron

NDC Code 0143-2423-01
Proprietary Name Ondansetron
Package Description 100 TABLET in 1 BOTTLE, GLASS (0143-2423-01)
Product NDC 0143-2423
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Ondansetron hydrochloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20080101
Marketing Category Name ANDA
Labeler Name West-ward Pharmaceutical 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


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