Class II ยท Moderate risk
Atomoxetine Capsules HCL
Labeling: Label Mix-Up: Atomoxetine HCl 25mg Capsule incorrectly labeled as Atomoxetine HCl 10mg Capsule.
National Drug Code
Is NDC 64380-0474-01 recalled?
Atomoxetine · 30 CAPSULE in 1 BOTTLE, PLASTIC (64380-474-01)
Yes — this exact package was recalled
1 FDA recall names the code 64380-0474-01 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.
1 of these recalls is still ongoing.
- Active ingredient
- Atomoxetine
- Strength
- ATOMOXETINE HYDROCHLORIDE 25 mg/1
- Form
- Capsule · Oral
- Labeler
- Strides Pharma Science Limited
- Type
- Human Prescription Drug
- Product code
- 64380-0474
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
- 64380-0861 Potassium Chloride 2
- 64380-0933 LOSARTAN POTASSIUM 25 mg 2
- 64380-0151 Testosterone 1
- 64380-0152 Testosterone 1
- 64380-0713 Benzonatate 1
- 64380-0721 Tacrolimus 1
Free recall alerts
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