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Gentamicin Sulfate in Sodium Chloride - 0409-7889-23 - (GENTAMICIN SULFATE)

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Drug Information of Gentamicin Sulfate in Sodium Chloride

Product NDC: 0409-7889
Proprietary Name: Gentamicin Sulfate in Sodium Chloride
Non Proprietary Name: GENTAMICIN SULFATE
Active Ingredient(s): 1    mg/mL & nbsp;   GENTAMICIN SULFATE
Administration Route(s): INTRAVENOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Gentamicin Sulfate in Sodium Chloride

Product NDC: 0409-7889
Labeler Name: Hospira, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA062414
Marketing Category: ANDA
Start Marketing Date: 20091204

Package Information of Gentamicin Sulfate in Sodium Chloride

Package NDC: 0409-7889-23
Package Description: 24 POUCH in 1 CASE (0409-7889-23) > 1 BAG in 1 POUCH > 100 mL in 1 BAG

NDC Information of Gentamicin Sulfate in Sodium Chloride

NDC Code 0409-7889-23
Proprietary Name Gentamicin Sulfate in Sodium Chloride
Package Description 24 POUCH in 1 CASE (0409-7889-23) > 1 BAG in 1 POUCH > 100 mL in 1 BAG
Product NDC 0409-7889
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name GENTAMICIN SULFATE
Dosage Form Name INJECTION, SOLUTION
Route Name INTRAVENOUS
Start Marketing Date 20091204
Marketing Category Name ANDA
Labeler Name Hospira, Inc.
Substance Name GENTAMICIN SULFATE
Strength Number 1
Strength Unit mg/mL
Pharmaceutical Classes Aminoglycoside Antibacterial [EPC],Aminoglycosides [Chemical/Ingredient]

Complete Information of Gentamicin Sulfate in Sodium Chloride


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