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ALREX
ALREX - 24208-353-10 - (loteprednol etabonate)
Drug Information of ALREX
| Product NDC: | 24208-353 |
| Proprietary Name: | ALREX |
| Non Proprietary Name: | loteprednol etabonate |
| Active Ingredient(s): | 2 mg/mL & nbsp; loteprednol etabonate |
| Administration Route(s): | OPHTHALMIC |
| Dosage Form(s): | SUSPENSION/ DROPS |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of ALREX
| Product NDC: | 24208-353 |
| Labeler Name: | Bausch & Lomb Incorporated |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA020803 |
| Marketing Category: | NDA |
| Start Marketing Date: | 19980309 |
Package Information of ALREX
| Package NDC: | 24208-353-10 |
| Package Description: | 1 BOTTLE, DROPPER in 1 CARTON (24208-353-10) > 10 mL in 1 BOTTLE, DROPPER |
NDC Information of ALREX
| NDC Code | 24208-353-10 |
| Proprietary Name | ALREX |
| Package Description | 1 BOTTLE, DROPPER in 1 CARTON (24208-353-10) > 10 mL in 1 BOTTLE, DROPPER |
| Product NDC | 24208-353 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | loteprednol etabonate |
| Dosage Form Name | SUSPENSION/ DROPS |
| Route Name | OPHTHALMIC |
| Start Marketing Date | 19980309 |
| Marketing Category Name | NDA |
| Labeler Name | Bausch & Lomb Incorporated |
| Substance Name | LOTEPREDNOL ETABONATE |
| Strength Number | 2 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA] |
