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Gentamicin Sulfate - 0168-0071-15 - (gentamicin sulfate)

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Drug Information of Gentamicin Sulfate

Product NDC: 0168-0071
Proprietary Name: Gentamicin Sulfate
Non Proprietary Name: gentamicin sulfate
Active Ingredient(s): 1    mg/g & nbsp;   gentamicin sulfate
Administration Route(s): TOPICAL
Dosage Form(s): CREAM
Coding System: National Drug Codes(NDC)

Labeler Information of Gentamicin Sulfate

Product NDC: 0168-0071
Labeler Name: E. FOUGERA & CO., A division of Fougera Pharmaceuticals Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA062531
Marketing Category: ANDA
Start Marketing Date: 19840705

Package Information of Gentamicin Sulfate

Package NDC: 0168-0071-15
Package Description: 15 g in 1 TUBE (0168-0071-15)

NDC Information of Gentamicin Sulfate

NDC Code 0168-0071-15
Proprietary Name Gentamicin Sulfate
Package Description 15 g in 1 TUBE (0168-0071-15)
Product NDC 0168-0071
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name gentamicin sulfate
Dosage Form Name CREAM
Route Name TOPICAL
Start Marketing Date 19840705
Marketing Category Name ANDA
Labeler Name E. FOUGERA & CO., A division of Fougera Pharmaceuticals Inc.
Substance Name GENTAMICIN SULFATE
Strength Number 1
Strength Unit mg/g
Pharmaceutical Classes Aminoglycoside Antibacterial [EPC],Aminoglycosides [Chemical/Ingredient]

Complete Information of Gentamicin Sulfate


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