| Product NDC: | 24208-004 |
| Proprietary Name: | Istalol |
| Non Proprietary Name: | Timolol Maleate |
| Active Ingredient(s): | 6.8 mg/mL & nbsp; Timolol Maleate |
| Administration Route(s): | OPHTHALMIC |
| Dosage Form(s): | SOLUTION/ DROPS |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 24208-004 |
| Labeler Name: | Bausch & Lomb Incorporated |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA021516 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20040802 |
| Package NDC: | 24208-004-03 |
| Package Description: | 1 BOTTLE, DROPPER in 1 CARTON (24208-004-03) > 5 mL in 1 BOTTLE, DROPPER |
| NDC Code | 24208-004-03 |
| Proprietary Name | Istalol |
| Package Description | 1 BOTTLE, DROPPER in 1 CARTON (24208-004-03) > 5 mL in 1 BOTTLE, DROPPER |
| Product NDC | 24208-004 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Timolol Maleate |
| Dosage Form Name | SOLUTION/ DROPS |
| Route Name | OPHTHALMIC |
| Start Marketing Date | 20040802 |
| Marketing Category Name | NDA |
| Labeler Name | Bausch & Lomb Incorporated |
| Substance Name | TIMOLOL MALEATE |
| Strength Number | 6.8 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Adrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC] |