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According to a statement from Teva, the company is recalling 35 lots of bulk losartan potassium tablets (6 lots of 25 mg strength and 29 lots of 100 mg strength) because developers found NMBA in six lots of active pharmaceutical ingredient (API) manufactured by Hetero Labs Limited in India

This modified version was shown to have similar or even the same effects as

Eli Lilly is looking to create an alternative that offers a more sustainable, realistic ideal for its target audience, made even easier to integrate into daily life through a daily pill rather than a weekly shot

In the United States, BPC-157 is not FDA-approved and is sold as a research compound