Class II · Moderate risk
Nortriptyline HCL
Labeling: Label Mixup: NORTRIPTYLINE HCL, Capsule, 10 mg may have potentially been mislabeled as the following drug: VALSARTAN, Tablet, 80 mg, NDC 00078035834, Pedigree: AD70585_1, EXP: 5/29/2014.
National Drug Code
Is NDC 0093-0810-01 recalled?
Nortriptyline Hydrochloride · 100 CAPSULE in 1 BOTTLE (0093-0810-01)
Yes — this exact package was recalled
1 FDA recall names the code 0093-0810-01 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 10 mg/1
- Form
- Capsule · Oral
- Labeler
- Teva Pharmaceuticals USA, Inc.
- Type
- Human Prescription Drug
- Product code
- 0093-0810
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
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