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Zylet
Zylet - 24208-358-10 - (loteprednol etabonate and tobramycin)
Drug Information of Zylet
| Product NDC: | 24208-358 |
| Proprietary Name: | Zylet |
| Non Proprietary Name: | loteprednol etabonate and tobramycin |
| Active Ingredient(s): | 5; 3 mg/mL; mg/mL & nbsp; loteprednol etabonate and tobramycin |
| Administration Route(s): | OPHTHALMIC |
| Dosage Form(s): | SUSPENSION/ DROPS |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Zylet
| Product NDC: | 24208-358 |
| Labeler Name: | Bausch & Lomb Incorporated |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA050804 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20041214 |
Package Information of Zylet
| Package NDC: | 24208-358-10 |
| Package Description: | 1 BOTTLE, DROPPER in 1 CARTON (24208-358-10) > 10 mL in 1 BOTTLE, DROPPER |
NDC Information of Zylet
| NDC Code | 24208-358-10 |
| Proprietary Name | Zylet |
| Package Description | 1 BOTTLE, DROPPER in 1 CARTON (24208-358-10) > 10 mL in 1 BOTTLE, DROPPER |
| Product NDC | 24208-358 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | loteprednol etabonate and tobramycin |
| Dosage Form Name | SUSPENSION/ DROPS |
| Route Name | OPHTHALMIC |
| Start Marketing Date | 20041214 |
| Marketing Category Name | NDA |
| Labeler Name | Bausch & Lomb Incorporated |
| Substance Name | LOTEPREDNOL ETABONATE; TOBRAMYCIN |
| Strength Number | 5; 3 |
| Strength Unit | mg/mL; mg/mL |
| Pharmaceutical Classes | Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA],Aminoglycoside Antibacterial [EPC],Aminoglycosides [Chemical/Ingredient] |
