Class II ยท Moderate risk
Ramipril Capsules USP
Failed Impurities/Degradation Specifications: OOS result obtained for a process impurity, dicyclohexylurea (DCU).
National Drug Code
Is NDC 76282-0673-01 recalled?
Ramipril · 100 CAPSULE in 1 BOTTLE (76282-673-01)
Yes — this exact package was recalled
1 FDA recall names the code 76282-0673-01 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
- Ramipril
- Strength
- RAMIPRIL 10 mg/1
- Form
- Capsule · Oral
- Labeler
- Exelan Pharmaceuticals, Inc.
- Type
- Human Prescription Drug
- Product code
- 76282-0673
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
- 76282-0478 Lanthanum carbonate 2
- 76282-0103 Diclofenac Sodium 1
- 76282-0405 Gabapentin 1
- 76282-0708 See recall 1
Free recall alerts
Know the day your medication is recalled
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