Class III ยท Low risk
Lisinopril Tablets USP 20 mg
Presence of Foreign Tablets: Potential of stray tablet(s) of Amlodipine Besylate 10 mg Tablet within the recalled lots
National Drug Code
Is NDC 0615-8255-39 recalled?
Lisinopril · 30 TABLET in 1 BLISTER PACK (0615-8255-39)
Yes — this exact package was recalled
1 FDA recall names the code 0615-8255-39 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
- Lisinopril
- Strength
- LISINOPRIL 20 mg/1
- Form
- Tablet · Oral
- Labeler
- NCS HealthCare of KY, LLC dba Vangard Labs
- Type
- Human Prescription Drug
- Product code
- 0615-8255
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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