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Gentamicin Sulfate - 0409-3400-01 - (GENTAMICIN SULFATE)

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Drug Information of Gentamicin Sulfate

Product NDC: 0409-3400
Proprietary Name: Gentamicin Sulfate
Non Proprietary Name: GENTAMICIN SULFATE
Active Ingredient(s): 10    mg/mL & nbsp;   GENTAMICIN SULFATE
Administration Route(s): INTRAVENOUS
Dosage Form(s): INJECTION, SOLUTION, CONCENTRATE
Coding System: National Drug Codes(NDC)

Labeler Information of Gentamicin Sulfate

Product NDC: 0409-3400
Labeler Name: Hospira, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA062612
Marketing Category: ANDA
Start Marketing Date: 20111130

Package Information of Gentamicin Sulfate

Package NDC: 0409-3400-01
Package Description: 25 VIAL, PATENT DELIVERY SYSTEM in 1 TRAY (0409-3400-01) > 6 mL in 1 VIAL, PATENT DELIVERY SYSTEM

NDC Information of Gentamicin Sulfate

NDC Code 0409-3400-01
Proprietary Name Gentamicin Sulfate
Package Description 25 VIAL, PATENT DELIVERY SYSTEM in 1 TRAY (0409-3400-01) > 6 mL in 1 VIAL, PATENT DELIVERY SYSTEM
Product NDC 0409-3400
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name GENTAMICIN SULFATE
Dosage Form Name INJECTION, SOLUTION, CONCENTRATE
Route Name INTRAVENOUS
Start Marketing Date 20111130
Marketing Category Name ANDA
Labeler Name Hospira, Inc.
Substance Name GENTAMICIN SULFATE
Strength Number 10
Strength Unit mg/mL
Pharmaceutical Classes Aminoglycoside Antibacterial [EPC],Aminoglycosides [Chemical/Ingredient]

Complete Information of Gentamicin Sulfate


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