Product NDC: | 54868-6287 |
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: | 54868-6287 |
Labeler Name: | Physicians Total Care, Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA076260 |
Marketing Category: | ANDA |
Start Marketing Date: | 20110725 |
Package NDC: | 54868-6287-1 |
Package Description: | 1 BOTTLE, DROPPER in 1 CARTON (54868-6287-1) > 10 mL in 1 BOTTLE, DROPPER |
NDC Code | 54868-6287-1 |
Proprietary Name | Brimonidine Tartrate |
Package Description | 1 BOTTLE, DROPPER in 1 CARTON (54868-6287-1) > 10 mL in 1 BOTTLE, DROPPER |
Product NDC | 54868-6287 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Brimonidine Tartrate |
Dosage Form Name | SOLUTION/ DROPS |
Route Name | OPHTHALMIC |
Start Marketing Date | 20110725 |
Marketing Category Name | ANDA |
Labeler Name | Physicians Total Care, Inc. |
Substance Name | BRIMONIDINE TARTRATE |
Strength Number | 2 |
Strength Unit | mg/mL |
Pharmaceutical Classes | Adrenergic alpha-Agonists [MoA],alpha-Adrenergic Agonist [EPC] |