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New Formulations of Omeprazole Delayed-Release Capsules Approved by FDA

PITTSBURGH, PA – June 2, 2003 – Mylan Laboratories Inc. (NYSE: MYL) announced today that the U.S. Food and Drug Administration (FDA) has granted final approval for its Abbreviated New Drug Application (ANDA) for Omeprazole Delayed-release Capsules, 10 mg and 20 mg strengths and tentative approval for the 40 mg strength.

Omeprazole Delayed-release Capsules is the generic version of AstraZeneca LP’s Prilosec®.

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