Independent register of U.S. FDA drug recalls · updated Oct 10, 2026
RxRecalls Get alerts

National Drug Code

Is NDC 0093-0813-01 recalled?

Nortriptyline Hydrochloride · 100 CAPSULE in 1 BOTTLE (0093-0813-01)

Yes — this exact package was recalled

1 FDA recall names the code 0093-0813-01 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
Nortriptyline Hydrochloride
Strength
NORTRIPTYLINE HYDROCHLORIDE 75 mg/1
Form
Capsule · Oral
Labeler
Teva Pharmaceuticals USA, Inc.
Type
Human Prescription Drug
Product code
0093-0813

Recalls naming this package

Class II · Moderate risk

Nortriptyline HCL

Labeling: Label Mixup: NORTRIPTYLINE HCL, Capsule, 75 mg may have potentially been mislabeled as one of the following drugs: guaiFENesin ER, Tablet, 600 mg, NDC 45802049878, Pedigree: AD21790_58, EXP: 5/1/2014; MIRTAZAPINE, Tablet, 7.5 mg, NDC 59762141509, Pedigree: W003693, EXP: 4/30/2014.

Terminated Labeling / mix-up Aidapak Services, LLC D-829-2014

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