Class II · Moderate risk
Ciprofloxacin Ophthalmic Solution USP
Defective container: Unable to get the solution out of the bottle as the spike of the cap was lodged in the nozzle of the product bottle
National Drug Code
Is NDC 69315-0308-10 recalled?
ciprofloxacin · 1 BOTTLE, PLASTIC in 1 CARTON (69315-308-10) / 10 mL in 1 BOTTLE, PLASTIC
Yes — this exact package was recalled
1 FDA recall names the code 69315-0308-10 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.
3 of these recalls are still ongoing.
- Active ingredient
- Ciprofloxacin
- Strength
- CIPROFLOXACIN HYDROCHLORIDE 3 mg/mL
- Form
- Solution · Ophthalmic
- Labeler
- Leading Pharma, LLC
- Type
- Human Prescription Drug
- Product code
- 69315-0308
Recalls naming this package
Class II · Moderate risk
Ciprofloxacin Ophthalmic Solution USP
Defective container: Unable to get the solution out of the bottle as the spike of the cap was lodged in the nozzle of the product bottle
Class II · Moderate risk
Ciprofloxacin ophthalmic solution USP
Defective container: unable to get the solution out of the bottle as the spike of the cap was lodged in the nozzle of the product bottle.
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
- 69315-0904 Lorazepam 2
- 69315-0118 Furosemide 1
- 69315-0127 Folic Acid 1
- 69315-0167 Clomipramine Hydrochloride 1
- 69315-0905 Lorazepam 1
- 69315-0906 Lorazepam 1
Free recall alerts
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