Bristol-Myers Squibb's Capoten (captopril)
Executive Summary
Approved Jan. 28 for use in patients with Type I insulin- dependent diabetes mellitus and retinopathy. FDA's Cardiovascular & Renal Drugs Advisory Committee recommended approval for the angiotensin-converting enzyme inhibitor following an Oct. 28 FDA Advisory Committee meeting ("The Pink Sheet" Nov. 1, 1993, T&G-7). Capoten received a positive endorsement from a BMS/National Institute of Diabetes & Digestive Kidney Diseases study published in the New England Journal of Medicine on Nov. 11 and more recently from a European study published in the Jan. 26 issue of Journal of the American Medical Association
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