July 23, 2003
Par Pharmaceutical Has Recalled
Amiloride Hydrochloride Tablets
The Food and Drug Administration (FDA) released the following information.
Amiloride Hydrochloride Tablets, USP, 5 mg, 100 tablet bottles, Rx only.
Recall # D-277-3.
Lot 035607; Expiration Date: 12/2004.
Par Pharmaceutical, Spring Valley, NY, by letters on May 30, 2003. Firm
initiated recall is ongoing.
Mislabeled; Bottle labeled as containing 5 mg Amiloride Hydrochloride
tablets actually contains Minoxidil 2.5 mg tablets.
VOLUME OF PRODUCT IN COMMERCE
4,821/100 count bottles.