Class II · Moderate risk
Brimonidine Tartrate/Timolol Maleate Ophthalmic Solution 0.2%/0.5%*
Lack of Assurance of Sterility
National Drug Code
Is NDC 60505-0589-02 recalled?
Brimonidine Tartrate/Timolol Maleate Ophthalmic Solution · 1 BOTTLE, DROPPER in 1 CARTON (60505-0589-2) / 10 mL in 1 BOTTLE, DROPPER
Yes — this exact package was recalled
1 FDA recall names the code 60505-0589-02 directly. A recall still applies to particular lot numbers — compare the lot on your package with the FDA notice below, and talk to your pharmacist before stopping a prescribed medication.
3 of these recalls are still ongoing.
- Active ingredient
- Brimonidine Tartrate and Timolol Maleate
- Strength
- BRIMONIDINE TARTRATE 2 mg/mL; TIMOLOL MALEATE 5 mg/mL
- Form
- Solution · Ophthalmic
- Labeler
- Apotex Corp.
- Type
- Human Prescription Drug
- Product code
- 60505-0589
Recalls naming this package
Class II · Moderate risk
Brimonidine Tartrate/Timolol Maleate Ophthalmic Solution
Lack of Assurance of Sterility; atypical weight loss due to improper bottle sealing leading to potential sterility concerns
Class II · Moderate risk
Brimonidine Tartrate/Timolol Maleate Ophthalmic Solution
Lack of Assurance of Sterility
Where to find this code. The NDC is printed on the pharmacy label and on the manufacturer's carton, usually as three groups of digits after “NDC”. The last group is the package size — two bottles of the same medicine can differ only in that group, and a recall may cover one but not the other.
Other recalled products from this labeler
- 60505-0829 Fluticasone Propionate 3
- 60505-2580 Atorvastatin Calcium 3
- 60505-0595 See recall 2
- 60505-0596 See recall 2
- 60505-0773 See recall 2
- 60505-1003 Ketorolac Tromethamine 2
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