Home > National Drug Code (NDC) > Triple Antibiotic

Triple Antibiotic - 52426-020-05 - (Bacitracin zinc, Neomycin sulfate, and Polymyxin B sulfate)

Alphabetical Index


Drug Information of Triple Antibiotic

Product NDC: 52426-020
Proprietary Name: Triple Antibiotic
Non Proprietary Name: Bacitracin zinc, Neomycin sulfate, and Polymyxin B sulfate
Active Ingredient(s): 400; 3.5; 5000    [iU]/g; mg/g; [iU]/g & nbsp;   Bacitracin zinc, Neomycin sulfate, and Polymyxin B sulfate
Administration Route(s): TOPICAL
Dosage Form(s): OINTMENT
Coding System: National Drug Codes(NDC)

Labeler Information of Triple Antibiotic

Product NDC: 52426-020
Labeler Name: Phoenix Global Supply Group, Inc
Product Type: HUMAN OTC DRUG
FDA Application Number: part333B
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20100923

Package Information of Triple Antibiotic

Package NDC: 52426-020-05
Package Description: 1 TUBE in 1 CARTON (52426-020-05) > 14.2 g in 1 TUBE

NDC Information of Triple Antibiotic

NDC Code 52426-020-05
Proprietary Name Triple Antibiotic
Package Description 1 TUBE in 1 CARTON (52426-020-05) > 14.2 g in 1 TUBE
Product NDC 52426-020
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Bacitracin zinc, Neomycin sulfate, and Polymyxin B sulfate
Dosage Form Name OINTMENT
Route Name TOPICAL
Start Marketing Date 20100923
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name Phoenix Global Supply Group, Inc
Substance Name BACITRACIN ZINC; 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


General Information