TERBUTALINE SULFATE | N017466 | SANOFI AVENTIS US LLC
| Petition | Type | Filed | Status | Petitioner |
|---|---|---|---|---|
Citizen Petition from ANDA Consultants FDA-2016-P-3162 · 4 docket documents ANDA Consultants filed this citizen petition on October 5, 2016, requesting that the FDA Commissioner designate Terbutaline Sulfate Tablets, 5 mg (ANDA 77-152, held by Lannett Holdings Inc.) as a reference listed drug to serve as the reference standard for bioequivalence testing in subsequent abbrev | Other | 2016-10-11 | Withdrawn | ANDA Consultants |
Citizen Petition from Hikma Farmaceutica of Portugal FDA-2007-P-0407 · 9 docket documents Hikma Farmaceutica of Portugal filed this citizen petition pursuant to 505(q) of the Federal Food, Drug and Cosmetic Act requesting that the FDA determine that Brethine (Terbutaline Sulfate Injection, USP), an approved reference listed drug marketed by aaiPharma under NDA 18-571, was voluntarily wit | 505(q) | 2008-06-13 | Granted | Hikma Farmaceutica of Portugal |
Source: Regulations.gov. FDA citizen petitions matched by application number.
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