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Gentamicin Sulfate in Sodium Chloride - 0338-0501-48 - (Gentamicin Sulfate)

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Drug Information of Gentamicin Sulfate in Sodium Chloride

Product NDC: 0338-0501
Proprietary Name: Gentamicin Sulfate in Sodium Chloride
Non Proprietary Name: Gentamicin Sulfate
Active Ingredient(s): 60    mg/100mL & 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: 0338-0501
Labeler Name: Baxter Healthcare Corporation
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA062373
Marketing Category: ANDA
Start Marketing Date: 19820907

Package Information of Gentamicin Sulfate in Sodium Chloride

Package NDC: 0338-0501-48
Package Description: 100 mL in 1 BAG (0338-0501-48)

NDC Information of Gentamicin Sulfate in Sodium Chloride

NDC Code 0338-0501-48
Proprietary Name Gentamicin Sulfate in Sodium Chloride
Package Description 100 mL in 1 BAG (0338-0501-48)
Product NDC 0338-0501
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Gentamicin Sulfate
Dosage Form Name INJECTION, SOLUTION
Route Name INTRAVENOUS
Start Marketing Date 19820907
Marketing Category Name ANDA
Labeler Name Baxter Healthcare Corporation
Substance Name GENTAMICIN SULFATE
Strength Number 60
Strength Unit mg/100mL
Pharmaceutical Classes Aminoglycoside Antibacterial [EPC],Aminoglycosides [Chemical/Ingredient]

Complete Information of Gentamicin Sulfate in Sodium Chloride


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