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Gentamicin Sulfate - 54868-6745-2 - (Gentamicin Sulfate)

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Drug Information of Gentamicin Sulfate

Product NDC: 54868-6745
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: 54868-6745
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA064048
Marketing Category: ANDA
Start Marketing Date: 19930917

Package Information of Gentamicin Sulfate

Package NDC: 54868-6745-2
Package Description: 1 BOTTLE, DROPPER in 1 CARTON (54868-6745-2) > 15 mL in 1 BOTTLE, DROPPER

NDC Information of Gentamicin Sulfate

NDC Code 54868-6745-2
Proprietary Name Gentamicin Sulfate
Package Description 1 BOTTLE, DROPPER in 1 CARTON (54868-6745-2) > 15 mL in 1 BOTTLE, DROPPER
Product NDC 54868-6745
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Gentamicin Sulfate
Dosage Form Name SOLUTION/ DROPS
Route Name OPHTHALMIC
Start Marketing Date 19930917
Marketing Category Name ANDA
Labeler Name Physicians Total Care, 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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