Product NDC: | 52125-509 |
Proprietary Name: | Brimonidine Tartrate |
Non Proprietary Name: | Brimonidine Tartrate |
Active Ingredient(s): | 2 mg/mL & nbsp; Brimonidine Tartrate |
Administration Route(s): | OPHTHALMIC |
Dosage Form(s): | SOLUTION/ DROPS |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 52125-509 |
Labeler Name: | REMEDYREPACK INC. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA076260 |
Marketing Category: | ANDA |
Start Marketing Date: | 20130624 |
Package NDC: | 52125-509-01 |
Package Description: | 10 mL in 1 BOTTLE, DROPPER (52125-509-01) |
NDC Code | 52125-509-01 |
Proprietary Name | Brimonidine Tartrate |
Package Description | 10 mL in 1 BOTTLE, DROPPER (52125-509-01) |
Product NDC | 52125-509 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Brimonidine Tartrate |
Dosage Form Name | SOLUTION/ DROPS |
Route Name | OPHTHALMIC |
Start Marketing Date | 20130624 |
Marketing Category Name | ANDA |
Labeler Name | REMEDYREPACK INC. |
Substance Name | BRIMONIDINE TARTRATE |
Strength Number | 2 |
Strength Unit | mg/mL |
Pharmaceutical Classes | Adrenergic alpha-Agonists [MoA],alpha-Adrenergic Agonist [EPC] |