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NEOMYCIN and POLYMYXIN B SULFATES and HYDROCORTISONE - 16590-169-10 - (NEOMYCIN SULFATE, POLYMYXIN B SULFATE, HYDROCORTISONE)

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Drug Information of NEOMYCIN and POLYMYXIN B SULFATES and HYDROCORTISONE

Product NDC: 16590-169
Proprietary Name: NEOMYCIN and POLYMYXIN B SULFATES and HYDROCORTISONE
Non Proprietary Name: NEOMYCIN SULFATE, POLYMYXIN B SULFATE, HYDROCORTISONE
Active Ingredient(s): 10; 3.5; 10000    mg/mL; mg/mL; [USP'U]/mL & nbsp;   NEOMYCIN SULFATE, POLYMYXIN B SULFATE, HYDROCORTISONE
Administration Route(s): AURICULAR (OTIC)
Dosage Form(s): SOLUTION/ DROPS
Coding System: National Drug Codes(NDC)

Labeler Information of NEOMYCIN and POLYMYXIN B SULFATES and HYDROCORTISONE

Product NDC: 16590-169
Labeler Name: STAT Rx USA LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA064053
Marketing Category: ANDA
Start Marketing Date: 19951229

Package Information of NEOMYCIN and POLYMYXIN B SULFATES and HYDROCORTISONE

Package NDC: 16590-169-10
Package Description: 1 BOTTLE, DROPPER in 1 CARTON (16590-169-10) > 10 mL in 1 BOTTLE, DROPPER

NDC Information of NEOMYCIN and POLYMYXIN B SULFATES and HYDROCORTISONE

NDC Code 16590-169-10
Proprietary Name NEOMYCIN and POLYMYXIN B SULFATES and HYDROCORTISONE
Package Description 1 BOTTLE, DROPPER in 1 CARTON (16590-169-10) > 10 mL in 1 BOTTLE, DROPPER
Product NDC 16590-169
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name NEOMYCIN SULFATE, POLYMYXIN B SULFATE, HYDROCORTISONE
Dosage Form Name SOLUTION/ DROPS
Route Name AURICULAR (OTIC)
Start Marketing Date 19951229
Marketing Category Name ANDA
Labeler Name STAT Rx USA LLC
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]

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