Sandoz Inc recalls Lisinopril Tablets USP, 30 mg, 100-count bottle, Rx Only, Manufactured by Sandoz Inc., Princeton, NJ 08540, NDC 0185-06…
- Recall date
- May 25, 2016
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Recall number
- D-1036-2016
- FDA classification
- Class III
- Brand / firm
- Sandoz Inc
- Sold / distributed
- Nationwide
Why it was recalled
Labeling: Incorrect or Missing Package Insert
Class III means the product violates regulations but is not likely to cause harm.
What was recalled
Lisinopril Tablets USP, 30 mg, 100-count bottle, Rx Only, Manufactured by Sandoz Inc., Princeton, NJ 08540, NDC 0185-0630-01
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