Product NDC: | 54868-3713 |
Proprietary Name: | Timolol Maleate |
Non Proprietary Name: | Timolol Maleate |
Active Ingredient(s): | 2.5 mg/mL & nbsp; Timolol Maleate |
Administration Route(s): | OPHTHALMIC |
Dosage Form(s): | SOLUTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 54868-3713 |
Labeler Name: | Physicians Total Care, Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA074261 |
Marketing Category: | ANDA |
Start Marketing Date: | 19960126 |
Package NDC: | 54868-3713-0 |
Package Description: | 10 mL in 1 BOTTLE, PLASTIC (54868-3713-0) |
NDC Code | 54868-3713-0 |
Proprietary Name | Timolol Maleate |
Package Description | 10 mL in 1 BOTTLE, PLASTIC (54868-3713-0) |
Product NDC | 54868-3713 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Timolol Maleate |
Dosage Form Name | SOLUTION |
Route Name | OPHTHALMIC |
Start Marketing Date | 19960126 |
Marketing Category Name | ANDA |
Labeler Name | Physicians Total Care, Inc. |
Substance Name | TIMOLOL MALEATE |
Strength Number | 2.5 |
Strength Unit | mg/mL |
Pharmaceutical Classes | Adrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC] |