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Ondansetron Hydrochloride - 0527-1726-41 - (Ondansetron Hydrochloride)

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Drug Information of Ondansetron Hydrochloride

Product NDC: 0527-1726
Proprietary Name: Ondansetron Hydrochloride
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 Hydrochloride

Product NDC: 0527-1726
Labeler Name: Lannett Company, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA090116
Marketing Category: ANDA
Start Marketing Date: 20100701

Package Information of Ondansetron Hydrochloride

Package NDC: 0527-1726-41
Package Description: 5 VIAL, SINGLE-DOSE in 1 CARTON (0527-1726-41) > 2 mL in 1 VIAL, SINGLE-DOSE

NDC Information of Ondansetron Hydrochloride

NDC Code 0527-1726-41
Proprietary Name Ondansetron Hydrochloride
Package Description 5 VIAL, SINGLE-DOSE in 1 CARTON (0527-1726-41) > 2 mL in 1 VIAL, SINGLE-DOSE
Product NDC 0527-1726
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Ondansetron Hydrochloride
Dosage Form Name INJECTION
Route Name INTRAMUSCULAR; INTRAVENOUS
Start Marketing Date 20100701
Marketing Category Name ANDA
Labeler Name Lannett Company, Inc.
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 Hydrochloride


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