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Ondansetron - 0143-2422-30 - (Ondansetron hydrochloride)

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Drug Information of Ondansetron

Product NDC: 0143-2422
Proprietary Name: Ondansetron
Non Proprietary Name: Ondansetron hydrochloride
Active Ingredient(s): 4    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: 0143-2422
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: 0143-2422-30
Package Description: 30 TABLET in 1 BOTTLE, PLASTIC (0143-2422-30)

NDC Information of Ondansetron

NDC Code 0143-2422-30
Proprietary Name Ondansetron
Package Description 30 TABLET in 1 BOTTLE, PLASTIC (0143-2422-30)
Product NDC 0143-2422
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 4
Strength Unit mg/1
Pharmaceutical Classes Serotonin 3 Receptor Antagonists [MoA],Serotonin-3 Receptor Antagonist [EPC]

Complete Information of Ondansetron


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