| Product NDC: | 61314-225 |
| Proprietary Name: | Timolol GFS |
| Non Proprietary Name: | timolol maleate |
| Active Ingredient(s): | 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: | 61314-225 |
| Labeler Name: | FALCON Pharmaceuticals, Ltd. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA020963 |
| Marketing Category: | NDA |
| Start Marketing Date: | 19981224 |
| Package NDC: | 61314-225-05 |
| Package Description: | 5 mL in 1 BOTTLE (61314-225-05) |
| NDC Code | 61314-225-05 |
| Proprietary Name | Timolol GFS |
| Package Description | 5 mL in 1 BOTTLE (61314-225-05) |
| Product NDC | 61314-225 |
| 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 | 5 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes |