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SafetyAlerts
November 12,  2003

Direct Dispensing Has Recalled INDOMETHACIN Capsules

(SafetyAlerts) - The FDA has released the following information.

PRODUCT
INDOMETHACIN Capsules, 25 MG, 60 capsule plastic bottles, RX ONLY. Recall # D-036-4.

CODE
Lot # 2I3981BB EXP 7/2004.

RECALLING FIRM/MANUFACTURER
Recalling Firm: Direct Dispensing, Inc., Miami, FL, by telephone, and letter on September 23, 2003.
Manufacturer: Mylan Pharamceuticals, Morgantown, WV.
FDA initiated recall is ongoing.

REASON
Label Mix-up: bottles labeled as containing 25 mg strength capsules actually contain 50 mg capsules.

VOLUME OF PRODUCT IN COMMERCE
400 bottles.

DISTRIBUTION
Nationwide
.

 
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During 2000 there were over
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The information contained herein has been obtained from sources that the Company believes to be reliable, however, the Company has not independently verified or confirmed the information and the recipient acknowledges that no representations or warranties are being made in connection with the use of the information.