Product NDC: | 61314-224 |
Proprietary Name: | Timolol GFS |
Non Proprietary Name: | timolol maleate |
Active Ingredient(s): | 2.5 mg/mL & nbsp; timolol maleate |
Administration Route(s): | OPHTHALMIC |
Dosage Form(s): | SOLUTION, GEL FORMING, EXTENDED RELEASE |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 61314-224 |
Labeler Name: | FALCON Pharmaceuticals, Ltd. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA020963 |
Marketing Category: | NDA |
Start Marketing Date: | 19981224 |
Package NDC: | 61314-224-05 |
Package Description: | 5 mL in 1 BOTTLE (61314-224-05) |
NDC Code | 61314-224-05 |
Proprietary Name | Timolol GFS |
Package Description | 5 mL in 1 BOTTLE (61314-224-05) |
Product NDC | 61314-224 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | timolol maleate |
Dosage Form Name | SOLUTION, GEL FORMING, EXTENDED RELEASE |
Route Name | OPHTHALMIC |
Start Marketing Date | 19981224 |
Marketing Category Name | NDA |
Labeler Name | FALCON Pharmaceuticals, Ltd. |
Substance Name | TIMOLOL MALEATE |
Strength Number | 2.5 |
Strength Unit | mg/mL |
Pharmaceutical Classes |