Recalls / Active ingredient / Naloxone Hydrochloride Dihydrate
Naloxone Hydrochloride Dihydrate
2 FDA drug recalls involving the active ingredient “Naloxone Hydrochloride Dihydrate”.
| Date | Class | Product | Firm |
|---|---|---|---|
| 2022-10-18 | Class II | Buprenorphine and Naloxone Sublingual Tablets 8 mg/2 mg, 30-count bottles, Rx only, Distributed by: Sun Phar | SUN PHARMACEUTICAL INDUSTRIES INC |
| 2021-02-26 | Class II | Buprenorphine and Naloxone Sublingual Film 2mg/0.5mg, 30 pouches each containing 1 sublingual film, Distribute | Alvogen, Inc |