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

Is NDC 0002-3250-30 recalled?

Strattera · 30 CAPSULE in 1 BOTTLE (0002-3250-30)

Yes — this exact package was recalled

1 FDA recall names the code 0002-3250-30 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
Atomoxetine hydrochloride
Strength
ATOMOXETINE HYDROCHLORIDE 80 mg/1
Form
Capsule · Oral
Labeler
Eli Lilly and Company
Type
Human Prescription Drug
Product code
0002-3250

Recalls naming this package

Class II ยท Moderate risk

Atomoxetine HCL

Labeling: Label Mixup: ATOMOXETINE HCL, Capsule, 80 mg may be potentially mis-labeled as one of the following drugs: ATOMOXETINE HCL, Capsule, 18 mg, NDC 00002323830, Pedigree: AD30140_16, EXP: 5/7/2014; PRENATAL MULTIVITAMIN/MULTIMINERAL, Tablet, 0 mg, NDC 00904531360, Pedigree: W003706, EXP: 6/25/2014; RANOLAZINE ER, Tablet, 500 mg, NDC 61958100301, Pedigree: AD60272_40, EXP: 5/22/2014; PRO

Terminated Labeling / mix-up Aidapak Services, LLC D-768-2014

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