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Triple Antibiotic Plus - 55301-823-56 - (bacitracin zinc,neomycin sulfate, polymyxin b sulfate, pramoxine hcl)

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Drug Information of Triple Antibiotic Plus

Product NDC: 55301-823
Proprietary Name: Triple Antibiotic Plus
Non Proprietary Name: bacitracin zinc,neomycin sulfate, polymyxin b sulfate, pramoxine hcl
Active Ingredient(s): 500; 3.5; 10000; 10    [USP'U]/g; mg/g; [USP'U]/g; mg/g & nbsp;   bacitracin zinc,neomycin sulfate, polymyxin b sulfate, pramoxine hcl
Administration Route(s): TOPICAL
Dosage Form(s): OINTMENT
Coding System: National Drug Codes(NDC)

Labeler Information of Triple Antibiotic Plus

Product NDC: 55301-823
Labeler Name: Exchange Select
Product Type: HUMAN OTC DRUG
FDA Application Number: part333B
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20050301

Package Information of Triple Antibiotic Plus

Package NDC: 55301-823-56
Package Description: 1 TUBE in 1 CARTON (55301-823-56) > 28 g in 1 TUBE

NDC Information of Triple Antibiotic Plus

NDC Code 55301-823-56
Proprietary Name Triple Antibiotic Plus
Package Description 1 TUBE in 1 CARTON (55301-823-56) > 28 g in 1 TUBE
Product NDC 55301-823
Product Type Name HUMAN OTC DRUG
Non Proprietary Name bacitracin zinc,neomycin sulfate, polymyxin b sulfate, pramoxine hcl
Dosage Form Name OINTMENT
Route Name TOPICAL
Start Marketing Date 20050301
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name Exchange Select
Substance Name BACITRACIN ZINC; NEOMYCIN SULFATE; POLYMYXIN B SULFATE; PRAMOXINE HYDROCHLORIDE
Strength Number 500; 3.5; 10000; 10
Strength Unit [USP'U]/g; mg/g; [USP'U]/g; mg/g
Pharmaceutical Classes

Complete Information of Triple Antibiotic Plus


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