Class II · Moderate risk
Aparaclonidine Ophthalmic Solution 0.5% as base
cGMP deviations: Temperature abuse
National Drug Code
Is NDC 61314-0665-05 recalled?
Apraclonidine · 5 mL in 1 BOTTLE (61314-665-05)
Yes — this exact package was recalled
1 FDA recall names the code 61314-0665-05 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
- Apraclonidine
- Strength
- APRACLONIDINE HYDROCHLORIDE 5.75 mg/mL
- Form
- Solution · Ophthalmic
- Labeler
- Sandoz Inc
- Type
- Human Prescription Drug
- Product code
- 61314-0665
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
- 61314-0656 Ciprofloxacin Hydrochloride 2
- 61314-0206 Pilocarpine Hydrochloride 1
- 61314-0630 Neomycin and Polymyxin B Sulfates and Dexamethasone 1
- 61314-0631 Neomycin and Polymyxin B Sulfates and Dexamethasone 1
- 61314-0637 Prednisolone Acetate 1
- 61314-0672 Gatifloxacin 1
Free recall alerts
Know the day your medication is recalled
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