NDC Code | 52125-602-08 |
Package Description | 10 mL in 1 BOTTLE, DROPPER (52125-602-08) |
Product NDC | 52125-602 |
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/ DROPS |
Usage | AURICULAR (OTIC) |
Start Marketing Date | 20140804 |
End Marketing Date | 20171116 |
Marketing Category Name | ANDA |
Application Number | ANDA064065 |
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] |