Class II ยท Moderate risk
CapsuleTOPRIL
Labeling: Label Mixup: CapsuleTOPRIL, Tablet, 25 mg may have potentially been mislabeled as the following drug: DULoxetine HCl DR, Capsule, 20 mg, NDC 00002323560, Pedigree AD54587_4, EXP: 5/21/2014.
National Drug Code
Is NDC 0143-1172-01 recalled?
Captopril · 100 TABLET in 1 BOTTLE (0143-1172-01)
Yes — this exact package was recalled
1 FDA recall names the code 0143-1172-01 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
- Captopril
- Strength
- CAPTOPRIL 25 mg/1
- Form
- Tablet · Oral
- Labeler
- Hikma Pharmaceuticals USA Inc.
- Type
- Human Prescription Drug
- Product code
- 0143-1172
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
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