Mylan Institutional, Inc. (d.b.a. UDL Laboratories) recalls Mirtazapine Tablets, USP, 45 mg. Rx only, 100 Tablets (10 X 10). Manufactured by: Mylan Pharmaceuticals Inc, Morgantown…
- Recall date
- January 27, 2017
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Recall number
- D-0493-2017
- FDA classification
- Class II
- Brand / firm
- Mylan Institutional, Inc. (d.b.a. UDL Laboratories)
- Sold / distributed
- Nationwide
Why it was recalled
Presence of Foreign Tablets/Capsules; possibility of Glipizide 10 mg tablets commingled
Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.
What was recalled
Mirtazapine Tablets, USP, 45 mg. Rx only, 100 Tablets (10 X 10). Manufactured by: Mylan Pharmaceuticals Inc, Morgantown, WV ---NDC 51079-088-20
Get recall alerts
Free email alert whenever Mylan Institutional, Inc. (d.b.a. UDL Laboratories) has a new recall — straight from official government data. Unsubscribe anytime.
More recalls from: Mylan Institutional, Inc. (d.b.a. UDL Laboratories)