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FDA Approves Four ANDAs for Sun Pharma
The FDA granted Sun Pharmaceutical Industries its first ANDA approval for a controlled substance, along with approvals for three additional generic drugs. The agency cleared the company’s hydro-codone bitartrate with acetaminophen (APAP) tablets and its generic formulations of Novartis’ Aredia (pamidronate disodium), Pfizer’s Lopid (gemfibrozil) and Wyeth’s Phenergan (promethazine HCl), India-based Sun says in a statement.
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