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Triple Antibiotic - 75934-0004-1 - (Neomycin Sulfate)

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Drug Information of Triple Antibiotic

Product NDC: 75934-0004
Proprietary Name: Triple Antibiotic
Non Proprietary Name: Neomycin Sulfate
Active Ingredient(s): 400; 3.5; 5000    [iU]/g; mg/g; [iU]/g & nbsp;   Neomycin Sulfate
Administration Route(s): TOPICAL
Dosage Form(s): OINTMENT
Coding System: National Drug Codes(NDC)

Labeler Information of Triple Antibiotic

Product NDC: 75934-0004
Labeler Name: Tiger Medical Group (US), Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number: part333B
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20120101

Package Information of Triple Antibiotic

Package NDC: 75934-0004-1
Package Description: 12 TUBE in 1 BOX (75934-0004-1) > 28 g in 1 TUBE

NDC Information of Triple Antibiotic

NDC Code 75934-0004-1
Proprietary Name Triple Antibiotic
Package Description 12 TUBE in 1 BOX (75934-0004-1) > 28 g in 1 TUBE
Product NDC 75934-0004
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Neomycin Sulfate
Dosage Form Name OINTMENT
Route Name TOPICAL
Start Marketing Date 20120101
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name Tiger Medical Group (US), Inc.
Substance Name BACITRACIN; NEOMYCIN SULFATE; POLYMYXIN B SULFATE
Strength Number 400; 3.5; 5000
Strength Unit [iU]/g; mg/g; [iU]/g
Pharmaceutical Classes

Complete Information of Triple Antibiotic


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