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Restasis Is FDA-Approved, Allergan Reminds Compounder

Law360, New York (January 11, 2018, 8:22 PM EST) -- Allergan USA Inc. on Wednesday urged a California federal court to shoot down false advertising counterclaims brought by drug compounder Imprimis Pharmaceuticals Inc., arguing that it’s factually true that its dry-eye medication Restasis is U.S. Food and Drug Administration-approved.

Allergan said Imprimis’ counterclaims are baseless, as its ads don’t feature the words “FDA-approved,” and even if they did, the statement is true. The counterclaims are in response to Allergan’s suit, which is using the Lanham Act to test the extent to which drug compounders can mass-produce...
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Case Information

Case Title

Allergan USA, Inc. v. Imprimis Pharmaceuticals, Inc.


Case Number

8:17-cv-01551

Court

California Central

Nature of Suit

Other Statutory Actions

Judge

David O. Carter

Date Filed

September 7, 2017

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