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GENTAMICIN SULFATE - 52125-461-01 - (gentamicin sulfate)

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Drug Information of GENTAMICIN SULFATE

Product NDC: 52125-461
Proprietary Name: GENTAMICIN SULFATE
Non Proprietary Name: gentamicin sulfate
Active Ingredient(s): 3    mg/mL & nbsp;   gentamicin sulfate
Administration Route(s): OPHTHALMIC
Dosage Form(s): SOLUTION/ DROPS
Coding System: National Drug Codes(NDC)

Labeler Information of GENTAMICIN SULFATE

Product NDC: 52125-461
Labeler Name: REMEDYREPACK INC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA062452
Marketing Category: ANDA
Start Marketing Date: 20130705

Package Information of GENTAMICIN SULFATE

Package NDC: 52125-461-01
Package Description: 5 mL in 1 BOTTLE (52125-461-01)

NDC Information of GENTAMICIN SULFATE

NDC Code 52125-461-01
Proprietary Name GENTAMICIN SULFATE
Package Description 5 mL in 1 BOTTLE (52125-461-01)
Product NDC 52125-461
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name gentamicin sulfate
Dosage Form Name SOLUTION/ DROPS
Route Name OPHTHALMIC
Start Marketing Date 20130705
Marketing Category Name ANDA
Labeler Name REMEDYREPACK INC.
Substance Name GENTAMICIN SULFATE
Strength Number 3
Strength Unit mg/mL
Pharmaceutical Classes Aminoglycoside Antibacterial [EPC],Aminoglycosides [Chemical/Ingredient]

Complete Information of GENTAMICIN SULFATE


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