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Ondansetron - 63323-374-20 - (ONDANSETRON HYDROCHLORIDE)

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Drug Information of Ondansetron

Product NDC: 63323-374
Proprietary Name: Ondansetron
Non Proprietary Name: ONDANSETRON HYDROCHLORIDE
Active Ingredient(s): 2    mg/mL & nbsp;   ONDANSETRON HYDROCHLORIDE
Administration Route(s): INTRAMUSCULAR; INTRAVENOUS
Dosage Form(s): INJECTION
Coding System: National Drug Codes(NDC)

Labeler Information of Ondansetron

Product NDC: 63323-374
Labeler Name: APP Pharmaceuticals, LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076974
Marketing Category: ANDA
Start Marketing Date: 20091118

Package Information of Ondansetron

Package NDC: 63323-374-20
Package Description: 1 VIAL in 1 BOX (63323-374-20) > 20 mL in 1 VIAL

NDC Information of Ondansetron

NDC Code 63323-374-20
Proprietary Name Ondansetron
Package Description 1 VIAL in 1 BOX (63323-374-20) > 20 mL in 1 VIAL
Product NDC 63323-374
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name ONDANSETRON HYDROCHLORIDE
Dosage Form Name INJECTION
Route Name INTRAMUSCULAR; INTRAVENOUS
Start Marketing Date 20091118
Marketing Category Name ANDA
Labeler Name APP Pharmaceuticals, LLC
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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