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2001 DEC 27 - (NewsRx.com & NewsRx.net) -- The U.S. Food and Drug Administration (FDA) has tentatively approved an Abbreviated New Drug Application (ANDA), filed by Gensia Sicor Pharmaceuticals, Inc., for pamidronate disodium for injection.
The active drug substance is manufactured and supplied by Sicor, Inc.'s wholly owned subsidiary, Sicor S.p.A. Pamidronate is used in the treatment of moderate or severe hypercalcemia associated with malignancy and moderate to severe Paget disease.
Based on data from IMS Health, a market research firm, U.S. sales of pamidronate in 2001 ...
Source: HighBeam Research, Gensia Sicor Gets Tentative ANDA Approval For Pamidronate Disodium...