Recalls / Active ingredient / Nalbuphine Hydrochloride
Nalbuphine Hydrochloride
1 FDA drug recall involving the active ingredient “Nalbuphine Hydrochloride”.
| Date | Class | Product | Firm |
|---|---|---|---|
| 2012-11-21 | Class II | Nalbuphine HCl Injection, 20 mg/mL, 10 mL Multiple-dose Fliptop Vial, Rx only, Hospira, Inc., Lake Forest, IL | Hospira, Inc. |