FDA Approval For Cetirizine Hydrochloride Tablets (OTC) ANDA - Hay Fever And Other Respiratory Allergies
Taro Pharmaceutical Industries Ltd. reported that it has received approval from the U.S. Food and Drug Administration (”FDA”) for its Abbreviated New Drug Application (”ANDA”) for cetirizine hydrochloride tablets (OTC), 5 mg and 10 mg (”Cetirizine Tablets”). The product will be marketed by Taro’s U.S. affiliate, Taro Pharmaceuticals U.S.A., Inc.
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August 24th, 2009 at 8:19 pm
madetyba…
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