Recalls / Active ingredient / Diphenoxylate Hydrochloride
Diphenoxylate Hydrochloride
1 FDA drug recall involving the active ingredient “Diphenoxylate Hydrochloride” — 1 Class I.
| Date | Class | Product | Firm |
|---|---|---|---|
| 2017-10-20 | Class I | diphenoxylate hydrochloride and atropine sulfate tablets, USP, 2.5 mg/0.025 mg, a) 100-count bottle (NDC 5976 | Pfizer Inc. |