KV Pharmaceutical Voluntarily Suspends All Shipments of its Approved Tablet-form Drugs

Date of Recall

2008-12-23

Recall Details

ST. LOUIS – Dec. 23, 2008 – KV Pharmaceutical has advised the U.S. Food and Drug Administration (FDA) that, effective midnight Dec. 19, 2008, the company voluntarily suspended all shipments of all FDA approved drug products in tablet form. KV Pharmaceutical is also recalling a single production lot of Hydromorphone HCl 2 mg tablets (Lot 90219, Exp: 3/2010; NDC 58177-0620-04), a pain management drug, following the report of an oversized tablet. Additional details on this recall were provided in an ETHEX Corporation press release also issued today and will be posted on www.kvpharmaceutical.com.

At this time, the company is unable to determine when distribution of tablet-form products will resume.

A full list of products included in the suspension of shipments can be viewed on the Company’s website at www.kvpharmaceutical.com, where a link can be found on the home page to “Products Effected by Shipment Suspension”.

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