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Ondansetron - 0143-9890-05 - (Ondansetron hydrochloride)

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Drug Information of Ondansetron

Product NDC: 0143-9890
Proprietary Name: Ondansetron
Non Proprietary Name: Ondansetron hydrochloride
Active Ingredient(s): 2    mg/mL & nbsp;   Ondansetron hydrochloride
Administration Route(s): INTRAVENOUS
Dosage Form(s): INJECTION
Coding System: National Drug Codes(NDC)

Labeler Information of Ondansetron

Product NDC: 0143-9890
Labeler Name: West-Ward Pharmaceutical Corp
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076780
Marketing Category: ANDA
Start Marketing Date: 20070101

Package Information of Ondansetron

Package NDC: 0143-9890-05
Package Description: 2 mL in 1 VIAL (0143-9890-05)

NDC Information of Ondansetron

NDC Code 0143-9890-05
Proprietary Name Ondansetron
Package Description 2 mL in 1 VIAL (0143-9890-05)
Product NDC 0143-9890
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Ondansetron hydrochloride
Dosage Form Name INJECTION
Route Name INTRAVENOUS
Start Marketing Date 20070101
Marketing Category Name ANDA
Labeler Name West-Ward Pharmaceutical Corp
Substance Name ONDANSETRON HYDROCHLORIDE
Strength Number 2
Strength Unit mg/mL
Pharmaceutical Classes Serotonin 3 Receptor Antagonists [MoA],Serotonin-3 Receptor Antagonist [EPC]

Complete Information of Ondansetron


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