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

Is NDC 39822-2000-01 recalled?

Clonidine · 10 mL in 1 VIAL, SINGLE-DOSE (39822-2000-1)

Yes — this exact package was recalled

2 FDA recalls name the code 39822-2000-01 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
Clonidine
Strength
CLONIDINE HYDROCHLORIDE 100 ug/mL
Form
Injection, Solution · Epidural
Labeler
XGen Pharmaceuticals DJB, Inc.
Type
Human Prescription Drug
Product code
39822-2000

Recalls naming this package

Class III · Low risk

Clonidine HCL Injection

Labeling: Label Error on Declared Strength: Side carton panel incorrectly lists the concentration as "500 mcg Clonidine Hydrochloride" rather than the correct concentration of "100 mcg Clonidine Hydrochloride" per mL.

Terminated Labeling / mix-up X-Gen Pharmaceuticals Inc. NDC 39822-2000-1 D-1084-2019
Class III · Low risk

Clonidine HCl Injection

Labeling: Label Error On Declared Strength: The side label description incorrectly states "Each mL contains 500 mcg Clonidine Hydrochloride" instead of stating "Each mL contains 100 mcg Clonidine Hydrochloride".

Terminated Labeling / mix-up X-Gen Pharmaceuticals Inc. NDC 39822-2000-1 D-1444-2014

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