Class II · Moderate risk
Creon DR 24
Lack of Processing Controls.
National Drug Code
Is NDC 0032-1224-01 recalled?
Creon · 100 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (0032-1224-01)
Yes — this exact package was recalled
1 FDA recall names the code 0032-1224-01 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.
- Active ingredient
- Pancrelipase
- Strength
- PANCRELIPASE LIPASE 24000 [USP'U]/1; PANCRELIPASE PROTEASE…
- Form
- Capsule, Delayed Release Pellets · Oral
- Labeler
- AbbVie Inc.
- Type
- Human Prescription Drug
- Product code
- 0032-1224
Recalls naming this package
Class II · Moderate risk
CREON (pancrelipase)
Presence of Foreign Tablets/Capsules; Presence of co-mingled LipaCreon 13000.
Class II · Moderate risk
Pancrelipase Dr
Labeling: Label Mixup: PANCRELIPASE DR, Capsule, 24000 /76000 /120000 USP units may be potentially mislabeled as one of the following drugs: SERTRALINE HCL, Tablet, 50 mg, NDC 16714061204, Pedigree: AD70585_7, EXP: 5/29/2014; THYROID, Tablet, 60 mg, NDC 00456045901, Pedigree: W002848, EXP: 6/7/2014; CHOLECALCIFEROL, Tablet, 2000 units, NDC 00904615760, Pedigree: W003744, EXP: 6/26/2014; amLOD
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
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