NDC 60505-0589
Brimonidine Tartrate/Timolol Maleate Ophthalmic Solution 2 mg per 1 mL / 5 mg per 1 mL solution
On the label: Apotex Corp..
Where it's made
This label doesn't name the factory that makes the drug. Companies don't have to print it on the label. The maker's name is often on the stock bottle your pharmacy used; you can ask the pharmacist. See the plants Apotex Corp. names for other drugs.
Recalls
- Mar 5, 2026 · Class II · Apotex Corp.
Lack of Assurance of Sterility
Lots: Lots VJ8599, Exp Date 09/30/2026 & VL1668, Exp Date 01/31/2027 - Sep 5, 2025 · Class II · Apotex Corp.
Lack of Assurance of Sterility; atypical weight loss due to improper bottle sealing leading to potential sterility concerns
Lots: a) lot # VE0614 exp. date 12/2025 UPC:(01)00360505058914 (5 mL) b) lot # VE0616 exp. date 12/2025 UPC:(01)0(03)60505058921 (10 mL) - May 28, 2025 · Class II · Apotex Corp.
Lack of Assurance of Sterility
Lots: Batch VC6058, Exp Date: 10/31/2025
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Brimonidine and Timolol: every company that makes it
- Form
- solution, ophthalmic
- Strength
- 2 mg per 1 mL / 5 mg per 1 mL
- Approval
- ANDA ANDA091442
- On the market since
- Oct 19, 2022
- Package NDCs
60505-0589-160505-0589-260505-0589-3- Official label
- DailyMed (National Library of Medicine), updated Apr 23, 2026
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?