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Brimonidine Tartrate - 52125-509-01 - (Brimonidine Tartrate)

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Drug Information of Brimonidine Tartrate

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)

Labeler Information of Brimonidine Tartrate

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 Information of Brimonidine Tartrate

Package NDC: 52125-509-01
Package Description: 10 mL in 1 BOTTLE, DROPPER (52125-509-01)

NDC Information of Brimonidine Tartrate

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]

Complete Information of Brimonidine Tartrate


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