Independent register of U.S. FDA drug recalls · updated Oct 10, 2026
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National Drug Code

Is NDC 60505-0564-01 recalled?

Brimonidine Tartrate · 1 BOTTLE, DROPPER in 1 CARTON (60505-0564-1) / 5 mL in 1 BOTTLE, DROPPER

Yes — this exact package was recalled

1 FDA recall names the code 60505-0564-01 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.

Active ingredient
brimonidine tartrate
Strength
BRIMONIDINE TARTRATE 1.5 mg/mL
Form
Solution/ Drops · Ophthalmic
Labeler
Apotex Corp.
Type
Human Prescription Drug
Product code
60505-0564

Recalls naming this package

Class II ยท Moderate risk

Brimonidine Tartrate Ophthalmic Solution 0.15%

Lack of sterility assurance: Cracks have developed in some of the units caps of Brimonidine tartrate ophthalmic solution bottles. There is a possibility the broken cap may impact sterility.

Completed Sterility / contamination Apotex Corp. NDC 60505-0564-1 D-0433-2023

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