Diovan (valsartan) 160 mg, 90 tablets, Rx only, Manufactured by: Patheon Manufacturing Services LLC, Greenville, NC 27834, Distributed by: Novartis Pharmaceutical Corp, East Hanover, NJ 07936, NDC 0078-0359-34
Failed Dissolution Specifications
| Recalling firm | Novartis Pharmaceuticals Corporation |
|---|---|
| Reason | Failed Dissolution Specifications |
| Risk class | Class II (Class II · moderate) |
| Status | Ongoing |
| Report date | Aug 19, 2026 |
| Initiated | Aug 4, 2026 |
| Region | NJ, United States |
| Distribution | US Nationwide |
| Code/Lot | Lot AV5913C, Expiry: 6/2027 |
| Type | Voluntary: Firm initiated |
| Recall number | D-0746-2026 |
Official source
U.S. FDA — Recalls, Market Withdrawals & Safety Alerts fda.gov ↗You can re-verify each item on the official FDA site using its recall number. (Recall number: D-0746-2026)
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