Itraconazole USP for prescription compounding recalled over manufacturing violations
- Recall date
- February 9, 2018
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Official notice title
- American Pharmaceutical Ingredients LLC recalls Itraconazole USP (Micronized) for prescription compounding, packaged in a) 10g (NDC 58597-8133-3); b) 25g (NDC 58597-81…
- Recall number
- D-0497-2018
- FDA classification
- Class II
- Brand / firm
- American Pharmaceutical Ingredients LLC
- Sold / distributed
- Nationwide within USA.
Why it was recalled
CGMP Deviations: Lack of stability data and controls to support the manufacturers assigned retest or expiration date in firm's container/closure system.
Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.
What was recalled
Itraconazole USP (Micronized) for prescription compounding, packaged in a) 10g (NDC 58597-8133-3); b) 25g (NDC 58597-8133-4); c)100g (NDC 58597-8133-6); d) 1000g (NDC 58597-8133-8), RX only, packed by American Pharmaceutical Ingredients, LLC 6650 Highland Road, Waterford, MI 48327
Get recall alerts
Free email alert whenever American Pharmaceutical Ingredients LLC has a new recall — straight from official government data. Unsubscribe anytime.
More recalls from: American Pharmaceutical Ingredients LLC