Class II · Moderate risk
National Drug Code
Is NDC 0023-9211-10 recalled?
Combigan · 1 BOTTLE, DROPPER in 1 CARTON (0023-9211-10) / 10 mL in 1 BOTTLE, DROPPER
Yes — this exact package was recalled
1 FDA recall names the code 0023-9211-10 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, timolol maleate
- Strength
- BRIMONIDINE TARTRATE 2 mg/mL; TIMOLOL MALEATE 5 mg/mL
- Form
- Solution/ Drops · Ophthalmic
- Labeler
- Allergan, Inc.
- Type
- Human Prescription Drug
- Product code
- 0023-9211
Recalls naming this package
Class III · Low risk
Combigan (brimonidine tartrate/timolol maleate ophthalmic solution)
Failed Impurities/Degradation Specifications.
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
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