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] |