Class II ยท Moderate risk
Lurasidone HCL
Labeling:Label Mixup; LURASIDONE HCl Tablet, 120 mg may be potentially mislabeled as DULoxetine HCl DR, Capsule, 20 mg, NDC 00002323560, Pedigree: W003486, EXP: 6/20/2014.
National Drug Code
Is NDC 63402-0312-30 recalled?
Latuda · 30 TABLET, FILM COATED in 1 BOTTLE (63402-312-30)
Yes — this exact package was recalled
1 FDA recall names the code 63402-0312-30 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
- lurasidone hydrochloride
- Strength
- LURASIDONE HYDROCHLORIDE 120 mg/1
- Form
- Tablet, Film Coated · Oral
- Labeler
- Sumitomo Pharma America, Inc.
- Type
- Human Prescription Drug
- Product code
- 63402-0312
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
- 63402-0193 See recall 1
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