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Brimonidine Tartrate - 61314-143-15 - (Brimonidine Tartrate)

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Drug Information of Brimonidine Tartrate

Product NDC: 61314-143
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
Coding System: National Drug Codes(NDC)

Labeler Information of Brimonidine Tartrate

Product NDC: 61314-143
Labeler Name: Falcon Pharmaceuticals, Ltd.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076254
Marketing Category: ANDA
Start Marketing Date: 20030917

Package Information of Brimonidine Tartrate

Package NDC: 61314-143-15
Package Description: 15 mL in 1 BOTTLE (61314-143-15)

NDC Information of Brimonidine Tartrate

NDC Code 61314-143-15
Proprietary Name Brimonidine Tartrate
Package Description 15 mL in 1 BOTTLE (61314-143-15)
Product NDC 61314-143
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Brimonidine Tartrate
Dosage Form Name SOLUTION
Route Name OPHTHALMIC
Start Marketing Date 20030917
Marketing Category Name ANDA
Labeler Name Falcon Pharmaceuticals, Ltd.
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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