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Gentamicin Sulfate - 55154-2392-8 - (Gentamicin Sulfate)

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Drug Information of Gentamicin Sulfate

Product NDC: 55154-2392
Proprietary Name: Gentamicin Sulfate
Non Proprietary Name: Gentamicin Sulfate
Active Ingredient(s): 40    mg/mL & nbsp;   Gentamicin Sulfate
Administration Route(s): INTRAMUSCULAR; INTRAVENOUS
Dosage Form(s): INJECTION, SOLUTION, CONCENTRATE
Coding System: National Drug Codes(NDC)

Labeler Information of Gentamicin Sulfate

Product NDC: 55154-2392
Labeler Name: Cardinal Health
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA062420
Marketing Category: ANDA
Start Marketing Date: 19830815

Package Information of Gentamicin Sulfate

Package NDC: 55154-2392-8
Package Description: 1 VIAL, SINGLE-DOSE in 1 BAG (55154-2392-8) > 2 mL in 1 VIAL, SINGLE-DOSE

NDC Information of Gentamicin Sulfate

NDC Code 55154-2392-8
Proprietary Name Gentamicin Sulfate
Package Description 1 VIAL, SINGLE-DOSE in 1 BAG (55154-2392-8) > 2 mL in 1 VIAL, SINGLE-DOSE
Product NDC 55154-2392
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Gentamicin Sulfate
Dosage Form Name INJECTION, SOLUTION, CONCENTRATE
Route Name INTRAMUSCULAR; INTRAVENOUS
Start Marketing Date 19830815
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 Sulfate


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