Product NDC: | 52125-512 |
Proprietary Name: | Dorzolamide Hydrochloride and Timolol Maleate |
Non Proprietary Name: | Dorzolamide Hydrochloride and Timolol Maleate |
Active Ingredient(s): | 20; 5 mg/mL; mg/mL & nbsp; Dorzolamide Hydrochloride and Timolol Maleate |
Administration Route(s): | OPHTHALMIC |
Dosage Form(s): | SOLUTION/ DROPS |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 52125-512 |
Labeler Name: | REMEDYREPACK INC. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA077847 |
Marketing Category: | ANDA |
Start Marketing Date: | 20130604 |
Package NDC: | 52125-512-01 |
Package Description: | 10 mL in 1 BOX (52125-512-01) |
NDC Code | 52125-512-01 |
Proprietary Name | Dorzolamide Hydrochloride and Timolol Maleate |
Package Description | 10 mL in 1 BOX (52125-512-01) |
Product NDC | 52125-512 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Dorzolamide Hydrochloride and Timolol Maleate |
Dosage Form Name | SOLUTION/ DROPS |
Route Name | OPHTHALMIC |
Start Marketing Date | 20130604 |
Marketing Category Name | ANDA |
Labeler Name | REMEDYREPACK INC. |
Substance Name | DORZOLAMIDE HYDROCHLORIDE; TIMOLOL MALEATE |
Strength Number | 20; 5 |
Strength Unit | mg/mL; mg/mL |
Pharmaceutical Classes | Carbonic Anhydrase Inhibitor [EPC],Carbonic Anhydrase Inhibitors [MoA],Adrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC] |