Class II · Moderate risk
Altaire Fluorescein Sodium with Proparacaine Hydrochloride Ophthalmic Solution
Lack of Assurance of Sterility
National Drug Code
Is NDC 59390-0205-05 recalled?
Fluorescein Sodium and Proparacaine Hydrochloride · 1 BOTTLE, DROPPER in 1 CARTON (59390-205-05) / 5 mL in 1 BOTTLE, DROPPER
Yes — this exact package was recalled
1 FDA recall names the code 59390-0205-05 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
- Fluorescein Sodium and Proparacaine Hydrochloride
- Strength
- FLUORESCEIN SODIUM 2.5 mg/mL; PROPARACAINE HYDROCHLORIDE 5…
- Form
- Solution/ Drops · Ophthalmic
- Labeler
- Altaire Pharmaceuticals Inc.
- Type
- Human Prescription Drug
- Product code
- 59390-0205
Recalls naming this package
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
- 59390-0144 See recall 3
- 59390-0175 See recall 3
- 59390-0217 Ciprofloxacin HCl Ophthalmic 3
- 59390-0141 See recall 2
- 59390-0142 See recall 2
- 59390-0143 See recall 2
Free recall alerts
Know the day your medication is recalled
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