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Gentamicin Sulfate - 49999-138-15 - (Gentamicin Sulfate)

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Drug Information of Gentamicin Sulfate

Product NDC: 49999-138
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: 49999-138
Labeler Name: Lake Erie Medical & Surgical Supply DBA Quality Care Products LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA064048
Marketing Category: ANDA
Start Marketing Date: 20120312

Package Information of Gentamicin Sulfate

Package NDC: 49999-138-15
Package Description: 1 BOTTLE, DROPPER in 1 CARTON (49999-138-15) > 15 mL in 1 BOTTLE, DROPPER

NDC Information of Gentamicin Sulfate

NDC Code 49999-138-15
Proprietary Name Gentamicin Sulfate
Package Description 1 BOTTLE, DROPPER in 1 CARTON (49999-138-15) > 15 mL in 1 BOTTLE, DROPPER
Product NDC 49999-138
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Gentamicin Sulfate
Dosage Form Name SOLUTION/ DROPS
Route Name OPHTHALMIC
Start Marketing Date 20120312
Marketing Category Name ANDA
Labeler Name Lake Erie Medical & Surgical Supply DBA Quality Care Products LLC
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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