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.
Reported: December 14, 2022 Initiated: December 5, 2022 #D-0077-2023
Product Description
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.
Reason for Recall
Subpotent Drug: repackaged product was recalled by the manufacturer for subpotency.
Details
- Recalling Firm
- RemedyRepack Inc.
- Units Affected
- 9 boxes
- Distribution
- Product was distributed to two different customers in MI.
- Location
- Indiana, PA
Frequently Asked Questions
What product 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.. Recalled by RemedyRepack Inc.. Units affected: 9 boxes.
Why was this product recalled? ▼
Subpotent Drug: repackaged product was recalled by the manufacturer for subpotency.
Which agency issued this recall? ▼
This recall was issued by the FDA Drug on December 14, 2022. Severity: Moderate. Recall number: D-0077-2023.
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