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Rewind to November 2004: the Food and Drug Administration (FDA) announces the addition of a “black box” warning to the labeling for the injectable contraceptive depot medroxyprogesterone acetate (DMPA, Depo-Provera, Pfizer, New York City and MedroxyPROGESTERone Injection, Teva Pharmaceuticals USA, North Wales, PA).

DMPA: Survey offers snapshot of shot use