Class III ยท Low risk
Nilotinib Capsules
Failed Tablet/Capsule Specifications: Observed OOS results at 6-months long-term stability condition for Description test and Appearance by Visual Inspection test.
National Drug Code
Is NDC 69097-0032-56 recalled?
Nilotinib
Yes — this exact package was recalled
1 FDA recall names the code 69097-0032-56 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
- Nilotinib
- Strength
- NILOTINIB 200 mg/1
- Form
- Capsule · Oral
- Labeler
- Cipla USA Inc.
- Type
- Human Prescription Drug
- Product code
- 69097-0032
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
- 69097-0341 Difluprednate 3
- 69097-0410 Cinacalcet 3
- 69097-0411 Cinacalcet 3
- 69097-0412 Cinacalcet 3
- 69097-0142 Albuterol Sulfate 2
- 69097-0537 Testosterone Cypionate 2
Free recall alerts
Know the day your medication is recalled
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