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Lotemax
Lotemax - 24208-443-35 - (loteprednol etabonate)
Drug Information of Lotemax
| Product NDC: | 24208-443 |
| Proprietary Name: | Lotemax |
| Non Proprietary Name: | loteprednol etabonate |
| Active Ingredient(s): | 5 mg/g & nbsp; loteprednol etabonate |
| Administration Route(s): | OPHTHALMIC |
| Dosage Form(s): | OINTMENT |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Lotemax
| Product NDC: | 24208-443 |
| Labeler Name: | Bausch & Lomb Incorporated |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA200738 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20110415 |
Package Information of Lotemax
| Package NDC: | 24208-443-35 |
| Package Description: | 1 TUBE in 1 CARTON (24208-443-35) > 3.5 g in 1 TUBE |
NDC Information of Lotemax
| NDC Code | 24208-443-35 |
| Proprietary Name | Lotemax |
| Package Description | 1 TUBE in 1 CARTON (24208-443-35) > 3.5 g in 1 TUBE |
| Product NDC | 24208-443 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | loteprednol etabonate |
| Dosage Form Name | OINTMENT |
| Route Name | OPHTHALMIC |
| Start Marketing Date | 20110415 |
| Marketing Category Name | NDA |
| Labeler Name | Bausch & Lomb Incorporated |
| Substance Name | LOTEPREDNOL ETABONATE |
| Strength Number | 5 |
| Strength Unit | mg/g |
| Pharmaceutical Classes | Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA] |
