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Brimonidine Tartrate - 61314-144-10 - (Brimonidine Tartrate)

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Drug Information of Brimonidine Tartrate

Product NDC: 61314-144
Proprietary Name: Brimonidine Tartrate
Non Proprietary Name: Brimonidine Tartrate
Active Ingredient(s): 1.5    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: 61314-144
Labeler Name: Falcon Pharmaceuticals, Ltd.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA021764
Marketing Category: NDA
Start Marketing Date: 20101002

Package Information of Brimonidine Tartrate

Package NDC: 61314-144-10
Package Description: 10 mL in 1 BOTTLE (61314-144-10)

NDC Information of Brimonidine Tartrate

NDC Code 61314-144-10
Proprietary Name Brimonidine Tartrate
Package Description 10 mL in 1 BOTTLE (61314-144-10)
Product NDC 61314-144
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Brimonidine Tartrate
Dosage Form Name SOLUTION
Route Name OPHTHALMIC
Start Marketing Date 20101002
Marketing Category Name NDA
Labeler Name Falcon Pharmaceuticals, Ltd.
Substance Name BRIMONIDINE TARTRATE
Strength Number 1.5
Strength Unit mg/mL
Pharmaceutical Classes Adrenergic alpha-Agonists [MoA],alpha-Adrenergic Agonist [EPC]

Complete Information of Brimonidine Tartrate


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