NDC 63629-8793

Brinzolamide

Brinzolamide

Brinzolamide is a Ophthalmic Suspension/ Drops in the Human Prescription Drug category. It is labeled and distributed by Bryant Ranch Prepack. The primary component is Brinzolamide.

Product ID63629-8793_3f6fee56-2754-465d-8631-13cb27eb6227
NDC63629-8793
Product TypeHuman Prescription Drug
Proprietary NameBrinzolamide
Generic NameBrinzolamide
Dosage FormSuspension/ Drops
Route of AdministrationOPHTHALMIC
Marketing Start Date2021-03-08
Marketing CategoryNDA AUTHORIZED GENERIC /
Application NumberNDA020816
Labeler NameBryant Ranch Prepack
Substance NameBRINZOLAMIDE
Active Ingredient Strength10 mg/mL
Pharm ClassesCarbonic Anhydrase Inhibitor [EPC],Carbonic Anhydrase Inhibitors [MoA]
NDC Exclude FlagN
Listing Certified Through2022-12-31

Packaging

NDC 63629-8793-1

1 BOTTLE, PLASTIC in 1 CARTON (63629-8793-1) > 10 mL in 1 BOTTLE, PLASTIC
Marketing Start Date2021-09-09
NDC Exclude FlagN
Sample Package?N

Drug Details

NDC Crossover Matching brand name "Brinzolamide" or generic name "Brinzolamide"

NDCBrand NameGeneric Name
0591-2127BrinzolamideBrinzolamide
0781-6014BrinzolamideBrinzolamide
24208-464BRINZOLAMIDEbrinzolamide
63629-8793BrinzolamideBrinzolamide
68682-464BRINZOLAMIDEbrinzolamide
0065-0275Azoptbrinzolamide
0078-0722Azoptbrinzolamide

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