| NDC Code | 50436-0736-1 |
|---|
| Package Description | 10 mL in 1 BOTTLE, DROPPER (50436-0736-1) |
|---|
| Product NDC | 50436-0736 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Neomycin And Polymyxin B Sulfates And Hydrocortisone |
|---|
| Non-Proprietary Name | Neomycin Sulfate, Polymyxin B Sulfate, Hydrocortisone |
|---|
| Dosage Form | SOLUTION/ DROPS |
|---|
| Usage | AURICULAR (OTIC) |
|---|
| Start Marketing Date | 19951229 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA064053 |
|---|
| Manufacturer | Unit Dose Services |
|---|
| Substance Name | NEOMYCIN SULFATE; POLYMYXIN B SULFATE; HYDROCORTISONE |
|---|
| Strength | 3.5; 10000; 10 |
|---|
| Strength Unit | mg/mL; [USP'U]/mL; mg/mL |
|---|
| Pharmacy Classes | Aminoglycoside Antibacterial [EPC],Aminoglycosides [Chemical/Ingredient],Polymyxin-class Antibacterial [EPC],Polymyxins [Chemical/Ingredient],Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA] |
|---|