| Product NDC: | 50383-021 |
| Proprietary Name: | Timolol Maleate |
| Non Proprietary Name: | Timolol Maleate |
| Active Ingredient(s): | 5 mg/mL & nbsp; Timolol Maleate |
| Administration Route(s): | OPHTHALMIC |
| Dosage Form(s): | SOLUTION/ DROPS |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 50383-021 |
| Labeler Name: | Hi-Tech Pharmacal Co., Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA075163 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20020910 |
| Package NDC: | 50383-021-10 |
| Package Description: | 1 BOTTLE in 1 CARTON (50383-021-10) > 10 mL in 1 BOTTLE |
| NDC Code | 50383-021-10 |
| Proprietary Name | Timolol Maleate |
| Package Description | 1 BOTTLE in 1 CARTON (50383-021-10) > 10 mL in 1 BOTTLE |
| Product NDC | 50383-021 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Timolol Maleate |
| Dosage Form Name | SOLUTION/ DROPS |
| Route Name | OPHTHALMIC |
| Start Marketing Date | 20020910 |
| Marketing Category Name | ANDA |
| Labeler Name | Hi-Tech Pharmacal Co., Inc. |
| Substance Name | TIMOLOL MALEATE |
| Strength Number | 5 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Adrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC] |