Gentamicin - 55154-9365-5 - (GENTAMICIN SULFATE)

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Drug Information of Gentamicin

Product NDC: 55154-9365
Proprietary Name: Gentamicin
Non Proprietary Name: GENTAMICIN SULFATE
Active Ingredient(s): 40    mg/mL & nbsp;   GENTAMICIN SULFATE
Administration Route(s): INTRAMUSCULAR; INTRAVENOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Gentamicin

Product NDC: 55154-9365
Labeler Name: Cardinal Health
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA062366
Marketing Category: ANDA
Start Marketing Date: 20000810

Package Information of Gentamicin

Package NDC: 55154-9365-5
Package Description: 5 VIAL in 1 BAG (55154-9365-5) > 2 mL in 1 VIAL

NDC Information of Gentamicin

NDC Code 55154-9365-5
Proprietary Name Gentamicin
Package Description 5 VIAL in 1 BAG (55154-9365-5) > 2 mL in 1 VIAL
Product NDC 55154-9365
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name GENTAMICIN SULFATE
Dosage Form Name INJECTION, SOLUTION
Route Name INTRAMUSCULAR; INTRAVENOUS
Start Marketing Date 20000810
Marketing Category Name ANDA
Labeler Name Cardinal Health
Substance Name GENTAMICIN SULFATE
Strength Number 40
Strength Unit mg/mL
Pharmaceutical Classes Aminoglycoside Antibacterial [EPC],Aminoglycosides [Chemical/Ingredient]

Complete Information of Gentamicin


General Information