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

Is NDC 65162-0713-10 recalled?

Guanfacine Hydrochloride · 100 TABLET in 1 BOTTLE (65162-713-10)

Yes — this exact package was recalled

1 FDA recall names the code 65162-0713-10 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.

Active ingredient
Guanfacine
Strength
GUANFACINE HYDROCHLORIDE 2 mg/1
Form
Tablet · Oral
Labeler
Amneal Pharmaceuticals LLC
Type
Human Prescription Drug
Product code
65162-0713

Recalls naming this package

Class II · Moderate risk

guanFACINE HCl Tablet

Labeling:Label Mixup; guanFACINE HCl Tablet, 2 mg may be potentially mislabeled as buPROPion HCl ER, Tablet, 200 mg, NDC 47335073886, Pedigree: AD21790_4, EXP: 5/1/2014; AMANTADINE HCL, Capsule, 100 mg, NDC 00781204801, Pedigree: W002997, EXP: 6/11/2014; glyBURIDE, Tablet, 1.25 mg, NDC 00093834201, Pedigree: W003677, EXP: 2/28/2014; ACYCLOVIR, Capsule, 200 mg, NDC 00093894001, Pedigree: AD60

Terminated Labeling / mix-up Aidapak Services, LLC D-711-2014

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