Class III · Low risk
Cequa (cyclosporine ophthalmic solution)
Subpotent: Out of Specification result observed for low assay
National Drug Code
Is NDC 47335-0506-96 recalled?
Cequa · 6 POUCH in 1 BOX (47335-506-96) / 10 VIAL, SINGLE-DOSE in 1 POUCH / .25 mL in 1 VIAL, SINGLE-DOSE
Yes — this exact package was recalled
4 FDA recalls name the code 47335-0506-96 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
- cyclosporine
- Strength
- CYCLOSPORINE .0009 g/mL
- Form
- Solution/ Drops · Ophthalmic, Topical
- Labeler
- Sun Pharmaceutical Industries, Inc.
- Type
- Human Prescription Drug
- Product code
- 47335-0506
Recalls naming this package
Class III · Low risk
Cequa (cyclosporine ophthalmic solution)
Subpotent Drug and Presence of Particulate Matter: low out-of-specification results obtained for assay and the presence of particulate matter.
Class III · Low risk
Cequa (cyclosporine ophthalmic solution)
Subpotent and Presence of Particulates .
Class III · Low risk
Cequa (cyclosporine ophthalmic solution)
Subpotent
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
- 47335-0737 Bupropion hydrochloride 6
- 47335-0738 Bupropion hydrochloride 5
- 47335-0063 Dofetilide 2
- 47335-0343 See recall 2
- 47335-0049 Doxorubicin Hydrochloride 1
- 47335-0154 See recall 1
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