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| L) reported that it has received final FDA approval for its Abbreviated New Drug Application (ANDA) and has started marketing its buspirone hydrochloride tablets in 5 mg, 10 mg and 15 mg strengths through the company's wholly owned subsidiary, IVAX Pharmaceuticals, Inc. Food and Drug Administration has approved the company's ANDA for Buspirone Hydrochloride Tablets USP, 5 mg, 10 mg and 15 mg. NYSE:MYL) announced today that it has received approval from the Food and Drug Administration to manufacture and market Buspirone Hydrochloride Tablets 30 mg. |
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