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BRIMONIDINE TARTRATE - 16590-883-10 - (BRIMONIDINE TARTRATE)

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Drug Information of BRIMONIDINE TARTRATE

Product NDC: 16590-883
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: 16590-883
Labeler Name: STAT RX USA LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076260
Marketing Category: ANDA
Start Marketing Date: 20030528

Package Information of BRIMONIDINE TARTRATE

Package NDC: 16590-883-10
Package Description: 10 mL in 1 BOTTLE, DROPPER (16590-883-10)

NDC Information of BRIMONIDINE TARTRATE

NDC Code 16590-883-10
Proprietary Name BRIMONIDINE TARTRATE
Package Description 10 mL in 1 BOTTLE, DROPPER (16590-883-10)
Product NDC 16590-883
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name BRIMONIDINE TARTRATE
Dosage Form Name SOLUTION/ DROPS
Route Name OPHTHALMIC
Start Marketing Date 20030528
Marketing Category Name ANDA
Labeler Name STAT RX USA LLC
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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