Product NDC: | 61314-226 |
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: | 61314-226 |
Labeler Name: | Falcon Pharmaceuticals, Ltd. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA074261 |
Marketing Category: | ANDA |
Start Marketing Date: | 19960115 |
Package NDC: | 61314-226-05 |
Package Description: | 5 mL in 1 BOTTLE, PLASTIC (61314-226-05) |
NDC Code | 61314-226-05 |
Proprietary Name | Timolol Maleate |
Package Description | 5 mL in 1 BOTTLE, PLASTIC (61314-226-05) |
Product NDC | 61314-226 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Timolol Maleate |
Dosage Form Name | SOLUTION |
Route Name | OPHTHALMIC |
Start Marketing Date | 19960115 |
Marketing Category Name | ANDA |
Labeler Name | Falcon Pharmaceuticals, Ltd. |
Substance Name | TIMOLOL MALEATE |
Strength Number | 2.5 |
Strength Unit | mg/mL |
Pharmaceutical Classes |