BRINZOLAMIDE 10 mg/mL
brinzolamide · SUSPENSION/ DROPS · Bausch & Lomb Incorporated
No Recall History
Plain English
BRINZOLAMIDE is a suspension/ drops containing brinzolamide at 10 mg/mL, taken ophthalmic. Manufactured by Bausch & Lomb Incorporated.
Key Facts
- Brand Name
- BRINZOLAMIDE
- Generic Name
- brinzolamide
- NDC Code (Product)
24208-464- Manufacturer
- Bausch & Lomb Incorporated
- Strength
- 10 mg/mL
- Dosage Form
- SUSPENSION/ DROPS
- Route
- OPHTHALMIC
- Marketing Status
- Application #
- ANDA204884
- Drug Class
- Carbonic Anhydrase Inhibitor [EPC]
- Marketing Start
- 03/31/2022
Recall History
No Recall HistorySide Effects Reported to FDA
FDA FAERS database · These are reported events, not confirmed side effects
dizziness313 reports
dyspnoea300 reports
fall272 reports
eye pain267 reports
diarrhoea262 reports
pruritus249 reports
arthralgia248 reports
headache241 reports
malaise240 reports
haemorrhagic stroke239 reports
Frequently Asked Questions
What is BRINZOLAMIDE used for?
BRINZOLAMIDE contains brinzolamide. It is a suspension/ drops taken ophthalmic. Consult your doctor for specific uses.
Is BRINZOLAMIDE a controlled substance?
BRINZOLAMIDE is not classified as a controlled substance by the DEA.
What is the generic name for BRINZOLAMIDE?
The generic name for BRINZOLAMIDE is brinzolamide. There are 3 other brand versions of brinzolamide.
What is the NDC code for BRINZOLAMIDE 10 mg/mL?
The NDC (National Drug Code) for BRINZOLAMIDE 10 mg/mL is 24208-464, listed by Bausch & Lomb Incorporated.