Lamivudine was invented by Bernard Belleau and Nghe Nguyen-Ba at the Montreal-based IAF BioChem International, Inc. laboratories in 1989. The drug was later licensed to the British pharmaceutical company Glaxo for a 14 percent royalty.

Following this, lamivudine was approved by the Food and Drug Administration (FDA) on November 17th 1995 for use with Zidovudine (AZT®) and again in 2002 as a once-a-day dosed medication. The fifth antiretroviral drug on the market, it was the last NRTI for three years while the approval process switched to protease inhibitors. Its patent will expire in the United States on 2016-05-18.

Please visit the official site of the FDA for further information.

 

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In case of an emergency/overdose