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14 Warning Letters Issued Over DMBA Presence in Supplements

The Food and Drug Administration (FDA) has issued warning letters to fourteen manufacturers of dietary supplements due to the listing of 1,3-Dimethylbutylamine (also known as DMBA, 2-amino-4-methylpentane, AMP citrate, and 4-methyl-2-pentanamine) on the product label.
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Agila Recalls Etomidate Injection Vials

Mylan announced that its subsidiary Agila Specialties is conducting a nationwide recall of 10 lots of Etomidate Injection 2mg/mL.