NDC 63629-8792

Brimonidine Tartrate

Brimonidine Tartrate

Brimonidine Tartrate is a Ophthalmic Solution in the Human Prescription Drug category. It is labeled and distributed by Bryant Ranch Prepack. The primary component is Brimonidine Tartrate.

Product ID63629-8792_74facda0-7b4e-4f52-9fc7-0926eb5b3fe4
NDC63629-8792
Product TypeHuman Prescription Drug
Proprietary NameBrimonidine Tartrate
Generic NameBrimonidine Tartrate
Dosage FormSolution
Route of AdministrationOPHTHALMIC
Marketing Start Date2010-10-02
Marketing CategoryNDA /
Application NumberNDA021764
Labeler NameBryant Ranch Prepack
Substance NameBRIMONIDINE TARTRATE
Active Ingredient Strength2 mg/mL
Pharm ClassesAdrenergic alpha-Agonists [MoA],alpha-Adrenergic Agonist [EPC]
NDC Exclude FlagN
Listing Certified Through2022-12-31

Packaging

NDC 63629-8792-1

5 mL in 1 BOTTLE (63629-8792-1)
Marketing Start Date2021-09-09
NDC Exclude FlagN
Sample Package?N

Drug Details

NDC Crossover Matching brand name "Brimonidine Tartrate" or generic name "Brimonidine Tartrate"

NDCBrand NameGeneric Name
14445-400Brimonidine TartrateBrimonidine Tartrate
24208-411Brimonidine TartrateBrimonidine Tartrate
25685-715Brimonidine Tartratebrimonidine tartrate
42843-501Brimonidine TartrateBrimonidine Tartrate
50090-1800Brimonidine TartrateBrimonidine Tartrate
50090-4224Brimonidine TartrateBrimonidine Tartrate
60505-0564Brimonidine Tartratebrimonidine tartrate
61314-143Brimonidine TartrateBrimonidine Tartrate
61314-144Brimonidine TartrateBrimonidine Tartrate
63629-8792Brimonidine TartrateBrimonidine Tartrate
70069-233BRIMONIDINE TARTRATEBRIMONIDINE TARTRATE
70069-232BRIMONIDINE TARTRATEBRIMONIDINE TARTRATE
70069-231BRIMONIDINE TARTRATEBRIMONIDINE TARTRATE
0023-9177ALPHAGAN Pbrimonidine tartrate
0023-9321ALPHAGAN Pbrimonidine tartrate
17478-715BrimonidineBrimonidine Tartrate
50090-1046BrimonidineBrimonidine Tartrate
24208-537LUMIFY Redness Reliever Eye DropsBRIMONIDINE TARTRATE
0299-5980Mirvasobrimonidine tartrate

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.