FUROSEMIDE | A075241 | HOSPIRA INC
| Petition | Type | Filed | Status | Petitioner |
|---|---|---|---|---|
Citizen Petition from Foley & Lardner LLP FDA-2018-P-1980 · 5 docket documents Foley & Lardner LLP filed this citizen petition under 21 CFR § 10.30 requesting that the FDA Commissioner designate Furosemide Injection 10 mg/mL, ANDA 075241 by Hospira, Inc., as a reference listed drug in the Orange Book to serve as a basis for filing additional Abbreviated New Drug Applications, | 505(q) | 2018-05-23 | Open | Foley & Lardner LLP |
Source: Regulations.gov. FDA citizen petitions matched by application number.
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