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Neomycin and Polymyxin B Sulfates and Hydrocortisone - 61314-645-11 - (neomycin sulfate, polymyxin b sulfate and hydrocortisone)

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Drug Information of Neomycin and Polymyxin B Sulfates and Hydrocortisone

Product NDC: 61314-645
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
Coding System: National Drug Codes(NDC)

Labeler Information of Neomycin and Polymyxin B Sulfates and Hydrocortisone

Product NDC: 61314-645
Labeler Name: Falcon Pharmaceuticals, Ltd.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA062488
Marketing Category: ANDA
Start Marketing Date: 20030317

Package Information of Neomycin and Polymyxin B Sulfates and Hydrocortisone

Package NDC: 61314-645-11
Package Description: 10 mL in 1 BOTTLE, PLASTIC (61314-645-11)

NDC Information of Neomycin and Polymyxin B Sulfates and Hydrocortisone

NDC Code 61314-645-11
Proprietary Name Neomycin and Polymyxin B Sulfates and Hydrocortisone
Package Description 10 mL in 1 BOTTLE, PLASTIC (61314-645-11)
Product NDC 61314-645
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name neomycin sulfate, polymyxin b sulfate and hydrocortisone
Dosage Form Name SUSPENSION
Route Name AURICULAR (OTIC)
Start Marketing Date 20030317
Marketing Category Name ANDA
Labeler Name Falcon Pharmaceuticals, Ltd.
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 Aminoglycoside Antibacterial [EPC],Aminoglycosides [Chemical/Ingredient],Polymyxin-class Antibacterial [EPC],Polymyxins [Chemical/Ingredient],Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA]

Complete Information of Neomycin and Polymyxin B Sulfates and Hydrocortisone


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