Class II · Moderate risk
Ramipril Capsules USP 2.5 mg
CGMP Deviations: Active pharmaceutical ingredient was sourced from an unapproved vendor
National Drug Code
Is NDC 68180-0589-02 recalled?
Ramipril · 500 CAPSULE in 1 BOTTLE (68180-589-02)
Yes — this exact package was recalled
1 FDA recall names the code 68180-0589-02 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
- Ramipril
- Strength
- RAMIPRIL 2.5 mg/1
- Form
- Capsule · Oral
- Labeler
- Lupin Pharmaceuticals, Inc.
- Type
- Human Prescription Drug
- Product code
- 68180-0589
Recalls naming this package
Class II · Moderate risk
Ramipril
Labeling:Label Mixup; RAMIPRIL, Capsule, 2.5 mg, Rx only may be potentially mislabeled as PROPAFENONE HCL, Tablet, 150 mg, NDC 00591058201, Pedigree: AD54549_13, EXP: 5/20/2014; CALCIUM POLYCARBOPHIL, Tablet, 625 mg, NDC 00536430611, Pedigree: AD73592_11, EXP: 5/31/2014.
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
- 68180-0723 Cefdinir 7
- 68180-0405 Cefixime 4
- 68180-0519 Lisinopril and Hydrochlorothiazide 4
- 68180-0422 Moxifloxacin 3
- 68180-0435 See recall 3
- 68180-0633 See recall 3
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