US Drug Recall Register
Class II · Moderate risk Terminated Initiated Dec 5, 2022 (4 years ago)

Desmopressin Acetate Tablet, 0.2 mg, 100-count box, Rx only, Source NDC: 23155-0490-01…

Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.

Why it was recalled

Subpotent Drug: repackaged product was recalled by the manufacturer for subpotency.

What was recalled

Desmopressin Acetate Tablet, 0.2 mg, 100-count box, Rx only, Source NDC: 23155-0490-01; MFG: Avet Pharmaceuticals Inc., East Brunswick, NJ 08816; Repackaged by: RemedyRepack Inc., Indiana, PA 15701, NDC #: 70518-3493-00.

Recalling firm
RemedyRepack Inc.
Origin
PA, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0077-2023

What should you do? A recall doesn't always mean your specific bottle is affected - it often applies to certain lots only. Check the lot number on your package against the FDA notice, and talk to your pharmacist before stopping any medication.

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