Class I ยท High risk
EliquisTablets 5mg
Labeling: Label Mix-up: One bottle of Eliquis 5 mg tablet was found to contain lower-strength Eliquis 2.5 mg tablets only instead of the labeled 5 mg tablets.
National Drug Code
Is NDC 0003-0894-21 recalled?
Eliquis · 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0003-0894-21)
Yes — this exact package was recalled
1 FDA recall names the code 0003-0894-21 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
- apixaban
- Strength
- APIXABAN 5 mg/1
- Form
- Tablet, Film Coated · Oral
- Labeler
- E.R. Squibb & Sons, L.L.C.
- Type
- Human Prescription Drug
- Product code
- 0003-0894
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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