| NDC Code | 52125-271-01 | 
|---|
			| Package Description | 10 mL in 1 BOTTLE, PLASTIC (52125-271-01) | 
|---|
			| Product NDC | 52125-271 | 
|---|
			| Product Type Name | HUMAN PRESCRIPTION DRUG | 
|---|
			| Proprietary Name | Neomycin And Polymyxin B Sulfates And Hydrocortisone | 
|---|
			
			| Non-Proprietary Name | Neomycin Sulfate, Polymyxin B Sulfate And Hydrocortisone | 
|---|
			| Dosage Form | SUSPENSION | 
|---|
			| Usage | AURICULAR (OTIC) | 
|---|
			| Start Marketing Date | 20130613 | 
|---|
			
			| Marketing Category Name | ANDA | 
|---|
			| Application Number | ANDA062488 | 
|---|
			| Manufacturer | REMEDYREPACK INC. | 
|---|
			| Substance Name | HYDROCORTISONE; NEOMYCIN SULFATE; POLYMYXIN B SULFATE | 
|---|
			| Strength | 10; 3.5; 10000 | 
|---|
			| Strength Unit | mg/mL; mg/mL; [USP'U]/mL | 
|---|
			| Pharmacy Classes | Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA],Aminoglycoside Antibacterial [EPC],Aminoglycosides [Chemical/Ingredient],Polymyxin-class Antibacterial [EPC],Polymyxins [Chemical/Ingredient] | 
|---|