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ondansetron hydrochloride - 25021-782-20 - (ondansetron hydrochloride)

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Drug Information of ondansetron hydrochloride

Product NDC: 25021-782
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): SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of ondansetron hydrochloride

Product NDC: 25021-782
Labeler Name: Sagent Pharmaceuticals
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA090648
Marketing Category: ANDA
Start Marketing Date: 20120830

Package Information of ondansetron hydrochloride

Package NDC: 25021-782-20
Package Description: 1 VIAL in 1 CARTON (25021-782-20) > 20 mL in 1 VIAL

NDC Information of ondansetron hydrochloride

NDC Code 25021-782-20
Proprietary Name ondansetron hydrochloride
Package Description 1 VIAL in 1 CARTON (25021-782-20) > 20 mL in 1 VIAL
Product NDC 25021-782
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name ondansetron hydrochloride
Dosage Form Name SOLUTION
Route Name INTRAMUSCULAR; INTRAVENOUS
Start Marketing Date 20120830
Marketing Category Name ANDA
Labeler Name Sagent Pharmaceuticals
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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