Class II ยท Moderate risk
Saphris 10 mg
Labeling; Label Mixup; blister lidding foil and shell-pack labeled as 10 mg but package actually contains 5 mg tablets
National Drug Code
Is NDC 0456-2410-60 recalled?
Saphris · 6 CASE in 1 CARTON (0456-2410-60) / 1 BLISTER PACK in 1 CASE (0456-2410-06) / 10 TABLET in 1 BLISTER PACK
Yes — this exact package was recalled
1 FDA recall names the code 0456-2410-60 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
- Asenapine Maleate
- Strength
- ASENAPINE MALEATE 10 mg/1
- Form
- Tablet · Sublingual
- Labeler
- Allergan, Inc.
- Type
- Human Prescription Drug
- Product code
- 0456-2410
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
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