Class II ยท Moderate risk
Atomoxetine Capsules
CGMP Deviations: presence of N-Nitroso Atomoxetine Impurity above the FDA recommended limit.
National Drug Code
Is NDC 16714-0755-01 recalled?
atomoxetine · 30 CAPSULE in 1 BOTTLE (16714-755-01)
Yes — this exact package was recalled
1 FDA recall names the code 16714-0755-01 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 10 mg/1
- Form
- Capsule · Oral
- Labeler
- Northstar Rx LLC
- Type
- Human Prescription Drug
- Product code
- 16714-0755
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
- 16714-0090 See recall 3
- 16714-0981 See recall 2
- 16714-0021 See recall 1
- 16714-0039 Colchicine 1
- 16714-0042 See recall 1
- 16714-0047 Chlorpromazine hydrochloride 1
Free recall alerts
Know the day your medication is recalled
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