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

Is NDC 70954-0912-10 recalled?

Hydroxyzine Hydrochloride · 473 mL in 1 BOTTLE (70954-912-10)

Yes — this exact package was recalled

1 FDA recall names the code 70954-0912-10 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
Hydroxyzine Hydrochloride
Strength
HYDROXYZINE DIHYDROCHLORIDE 10 mg/5mL
Form
Solution · Oral
Labeler
ANI Pharmaceuticals, Inc.
Type
Human Prescription Drug
Product code
70954-0912

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