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Neomycin and Polymyxin B Sulfates and Hydrocortisone - 52125-602-01 - (Neomycin sulfate, Polymyxin B Sulfate and Hydrocortisone)

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Drug Information of Neomycin and Polymyxin B Sulfates and Hydrocortisone

Product NDC: 52125-602
Proprietary Name: Neomycin and Polymyxin B Sulfates and Hydrocortisone
Non Proprietary Name: Neomycin sulfate, Polymyxin B Sulfate and Hydrocortisone
Active Ingredient(s): 10; 3.5; 10000    mg/mL; mg/mL; [USP'U]/mL & nbsp;   Neomycin sulfate, Polymyxin B Sulfate and Hydrocortisone
Administration Route(s): AURICULAR (OTIC)
Dosage Form(s): SUSPENSION/ DROPS
Coding System: National Drug Codes(NDC)

Labeler Information of Neomycin and Polymyxin B Sulfates and Hydrocortisone

Product NDC: 52125-602
Labeler Name: REMEDYREPACK INC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA064065
Marketing Category: ANDA
Start Marketing Date: 20130606

Package Information of Neomycin and Polymyxin B Sulfates and Hydrocortisone

Package NDC: 52125-602-01
Package Description: 10 mL in 1 CARTON (52125-602-01)

NDC Information of Neomycin and Polymyxin B Sulfates and Hydrocortisone

NDC Code 52125-602-01
Proprietary Name Neomycin and Polymyxin B Sulfates and Hydrocortisone
Package Description 10 mL in 1 CARTON (52125-602-01)
Product NDC 52125-602
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Neomycin sulfate, Polymyxin B Sulfate and Hydrocortisone
Dosage Form Name SUSPENSION/ DROPS
Route Name AURICULAR (OTIC)
Start Marketing Date 20130606
Marketing Category Name ANDA
Labeler Name REMEDYREPACK INC.
Substance Name HYDROCORTISONE; NEOMYCIN SULFATE; POLYMYXIN B SULFATE
Strength Number 10; 3.5; 10000
Strength Unit mg/mL; mg/mL; [USP'U]/mL
Pharmaceutical Classes Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA],Aminoglycoside Antibacterial [EPC],Aminoglycosides [Chemical/Ingredient],Polymyxin-class Antibacterial [EPC],Polymyxins [Chemical/Ingredient]

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