Class II · Moderate risk
CILOSTAZOL Tablet
Labeling:Label Mixup; CILOSTAZOL Tablet, 100 mg may be potentially mislabeled as DUTASTERIDE, Capsule, 0.5 mg, NDC 00173071204, Pedigree: AD65475_1, EXP: 5/28/2014.
National Drug Code
Is NDC 60505-2522-01 recalled?
cilostazol · 60 TABLET in 1 BOTTLE (60505-2522-1)
Yes — this exact package was recalled
2 FDA recalls name the code 60505-2522-01 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
- cilostazol
- Strength
- CILOSTAZOL 100 mg/1
- Form
- Tablet · Oral
- Labeler
- Apotex Corp.
- Type
- Human Prescription Drug
- Product code
- 60505-2522
Recalls naming this package
Class II · Moderate risk
CILOSTAZOL Tablet
Labeling:Label Mixup; CILOSTAZOL Tablet, 100 mg may be potentially mislabeled as DUTASTERIDE, Capsule, 0.5 mg, NDC 00173071204, Pedigree: AD65475_1, EXP: 5/28/2014.
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
- 60505-0589 Brimonidine Tartrate/Timolol Maleate Ophthalmic Solution 3
- 60505-0829 Fluticasone Propionate 3
- 60505-2580 Atorvastatin Calcium 3
- 60505-0595 See recall 2
- 60505-0596 See recall 2
- 60505-0773 See recall 2
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