| NDC Code | 70518-2198-0 |
|---|
| Package Description | 5 mL in 1 BOTTLE, PLASTIC (70518-2198-0) |
|---|
| Product NDC | 70518-2198 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Neomycin And Polymyxin B Sulfates And Dexamethasone |
|---|
| Non-Proprietary Name | Neomycin Sulfate, Polymyxin B Sulfate And Dexamethasone |
|---|
| Dosage Form | SUSPENSION |
|---|
| Usage | OPHTHALMIC |
|---|
| Start Marketing Date | 20190710 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA062341 |
|---|
| Manufacturer | REMEDYREPACK INC. |
|---|
| Substance Name | NEOMYCIN SULFATE; POLYMYXIN B SULFATE; DEXAMETHASONE |
|---|
| Strength | 3.5; 10000; 1 |
|---|
| Strength Unit | mg/mL; [USP'U]/mL; mg/mL |
|---|
| Pharmacy Classes | Aminoglycoside Antibacterial [EPC],Aminoglycosides [CS],Polymyxin-class Antibacterial [EPC],Polymyxins [CS],Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA] |
|---|