DIVALPROEX SODIUM | N019794 | ABBOTT LABORATORIES PHARMACEUTICAL PRODUCTS DIV
| Petition | Type | Filed | Status | Petitioner |
|---|---|---|---|---|
Citizen Petition from Abbott Laboratories (Clifford & Warnke) FDA-1986-P-0035 · 15 docket documents Abbott Laboratories filed this citizen petition on August 29, 1986, requesting that the FDA rule that DEPAKOTE (divalproex sodium) is entitled to ten years of exclusive marketing rights from its NDA approval date of March 10, 1983 (until March 10, 1993), and that the FDA refrain from making effectiv | 505(q) | 2025-11-06 | Denied | Abbott Laboratories (Clifford & Warnke) |
Source: Regulations.gov. FDA citizen petitions matched by application number.
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