Class II · Moderate risk
Ciprofloxacin Ophthalmic Solution 0.3%
cGMP deviations: Temperature abuse
National Drug Code
Is NDC 61314-0656-05 recalled?
Ciprofloxacin Hydrochloride · 1 BOTTLE, PLASTIC in 1 CARTON (61314-656-05) / 5 mL in 1 BOTTLE, PLASTIC
Yes — this exact package was recalled
1 FDA recall names the code 61314-0656-05 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
- Ciprofloxacin Hydrochloride
- Strength
- CIPROFLOXACIN HYDROCHLORIDE 3 mg/mL
- Form
- Solution/ Drops · Ophthalmic
- Labeler
- Sandoz Inc
- Type
- Human Prescription Drug
- Product code
- 61314-0656
Recalls naming this package
Class II · Moderate risk
Ciprofloxacin Ophthalmic Solution 0.3%
cGMP deviations: Temperature abuse
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
- 61314-0206 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
- 61314-0665 Apraclonidine 1
- 61314-0672 Gatifloxacin 1
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