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: | 24208-004-01 |
Package Description: | 1 BOTTLE, DROPPER in 1 CARTON (24208-004-01) > 2.5 mL in 1 BOTTLE, DROPPER |
NDC Code | 24208-004-01 |
Proprietary Name | Istalol |
Package Description | 1 BOTTLE, DROPPER in 1 CARTON (24208-004-01) > 2.5 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] |