Class II ยท Moderate risk
Preferred Pharmaceuticals
Out of specification results observed in dissolution during long term stability testing.
National Drug Code
Is NDC 68788-6390-09 recalled?
Lansoprazole · 90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68788-6390-9)
Yes — this exact package was recalled
1 FDA recall names the code 68788-6390-09 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
- lansoprazole
- Strength
- LANSOPRAZOLE 15 mg/1
- Form
- Capsule, Delayed Release · Oral
- Labeler
- Preferred Pharmaceuticals Inc.
- Type
- Human Prescription Drug
- Product code
- 68788-6390
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
- 68788-6932 See recall 3
- 68788-0048 See recall 2
- 68788-7758 See recall 2
- 68788-0841 See recall 1
- 68788-6381 See recall 1
- 68788-6382 See recall 1
Free recall alerts
Know the day your medication is recalled
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