Independent register of U.S. FDA drug recalls · updated Oct 10, 2026
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National Drug Code

Is NDC 0085-2224-02 recalled?

Noxafil · 8 PACKET in 1 CARTON (0085-2224-02) / 1 POWDER, FOR SUSPENSION in 1 PACKET (0085-2224-01)

Yes — this exact package was recalled

1 FDA recall names the code 0085-2224-02 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.

1 of these recalls is still ongoing.

Active ingredient
posaconazole
Strength
POSACONAZOLE 300 mg/1
Form
Powder, for Suspension · Oral
Labeler
Merck Sharp & Dohme LLC
Type
Human Prescription Drug
Product code
0085-2224

Recalls naming this package

Class II ยท Moderate risk

Noxafil Powdermix

Presence of particulate matter: potential presence of metal particulates in the product.

Ongoing Particulate / foreign matter Merck Sharp & Dohme LLC NDC 0085-2224-02 D-0242-2026

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