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ONDANSETRON HYDROCHLORIDE - 62756-181-01 - (ONDANSETRON HYDROCHLORIDE)

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Drug Information of ONDANSETRON HYDROCHLORIDE

Product NDC: 62756-181
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: 62756-181
Labeler Name: Sun Pharmaceutical Industries Limited
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077173
Marketing Category: ANDA
Start Marketing Date: 20061226

Package Information of ONDANSETRON HYDROCHLORIDE

Package NDC: 62756-181-01
Package Description: 5 AMPULE in 1 CARTON (62756-181-01) > 2 mL in 1 AMPULE

NDC Information of ONDANSETRON HYDROCHLORIDE

NDC Code 62756-181-01
Proprietary Name ONDANSETRON HYDROCHLORIDE
Package Description 5 AMPULE in 1 CARTON (62756-181-01) > 2 mL in 1 AMPULE
Product NDC 62756-181
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name ONDANSETRON HYDROCHLORIDE
Dosage Form Name INJECTION
Route Name INTRAMUSCULAR; INTRAVENOUS
Start Marketing Date 20061226
Marketing Category Name ANDA
Labeler Name Sun Pharmaceutical Industries Limited
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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