Praluent

Active Ingredient(s): Alirocumab
FDA Approved: * July 24, 2015
Pharm Company: * SANOFI AVENTIS
Category: Cholesterol

* This drug may consist of multiple approval dates, manufacturers, or distributors. If applicable, they would be listed below under "NDC Database Records".

Praluent Overview

Alirocumab (trade name Praluent)[1] is a biopharmaceutical drug approved by the FDA on July 24, 2015 as a second line treatment for high cholesterol for adults whose cholesterol is not controlled by diet and statin treatment. It is a human monoclonal antibody that belongs to a novel class of anti-cholesterol drugs, known as PCSK9 inhibitors, and it was the first such agent to receive FDA approval. The FDA approval was contingent on the completion of further clinical trials...

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Details May Include Instructions, Side Effects, Interactions, Etc. Drug monograph is from Wikipedia. All text is available under the terms of the GFDL (GNU Free Documentation License). Source: en.wikipedia.org/wiki/Alirocumab

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NDC Database Records for Praluent: (6 results)

Sorted by National Drug Code

• 0024-5901 Praluent 75 mg/ml Subcutaneous Injection, Solution by Sanofi-aventis U.S. LLC
• 0024-5902 Praluent 150 mg/ml Subcutaneous Injection, Solution by Sanofi-aventis U.S. LLC
• 0024-5903 Praluent 75 mg/ml Subcutaneous Injection, Solution by Sanofi-aventis U.S. LLC
• 0024-5904 Praluent 150 mg/ml Subcutaneous Injection, Solution by Sanofi-aventis U.S. LLC
• 72733-5901 Praluent 75 mg/ml Subcutaneous Injection, Solution by Sanofi Us Corporation
• 72733-5902 Praluent 150 mg/ml Subcutaneous Injection, Solution by Sanofi Us Corporation

Other drugs which contain Alirocumab or a similar ingredient: (1 result)

• ALIROCUMAB