| NDC Code | 71384-502-03 |
|---|
| Package Description | 20 BOTTLE, DROPPER in 1 BOX (71384-502-03) > 3.5 mL in 1 BOTTLE, DROPPER |
|---|
| Product NDC | 71384-502 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Pred-gati |
|---|
| Non-Proprietary Name | Prednisolone Acetate-gatifloxacin |
|---|
| Dosage Form | SUSPENSION/ DROPS |
|---|
| Usage | OPHTHALMIC |
|---|
| Start Marketing Date | 20180105 |
|---|
| Marketing Category Name | UNAPPROVED DRUG OTHER |
|---|
| Manufacturer | Imprimis NJOF, LLC |
|---|
| Substance Name | GATIFLOXACIN; PREDNISOLONE ACETATE |
|---|
| Strength | 5; 10 |
|---|
| Strength Unit | mg/mL; mg/mL |
|---|
| Pharmacy Classes | Quinolone Antimicrobial [EPC],Quinolones [CS],Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA] |
|---|