NDC Code | 70518-0864-0 |
Package Description | 10 mL in 1 BOTTLE, DROPPER (70518-0864-0) |
Product NDC | 70518-0864 |
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 | 20171124 |
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 | Aminoglycoside Antibacterial [EPC], Aminoglycosides [CS], Corticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC], Polymyxin-class Antibacterial [EPC], Polymyxins [CS] |