| Product NDC: | 60758-802 |
| 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/ DROPS |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 60758-802 |
| Labeler Name: | Pacific Pharma, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA074746 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 19970520 |
| Package NDC: | 60758-802-05 |
| Package Description: | 1 BOTTLE, DROPPER in 1 CARTON (60758-802-05) > 5 mL in 1 BOTTLE, DROPPER |
| NDC Code | 60758-802-05 |
| Proprietary Name | TIMOLOL MALEATE |
| Package Description | 1 BOTTLE, DROPPER in 1 CARTON (60758-802-05) > 5 mL in 1 BOTTLE, DROPPER |
| Product NDC | 60758-802 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | timolol maleate |
| Dosage Form Name | SOLUTION/ DROPS |
| Route Name | OPHTHALMIC |
| Start Marketing Date | 19970520 |
| Marketing Category Name | ANDA |
| Labeler Name | Pacific Pharma, Inc. |
| Substance Name | TIMOLOL MALEATE |
| Strength Number | 2.5 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Adrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC] |