A warning . . .

Joanne writes in with a warning . . .  

From The FDA Enforcement Report
1/30/08
PRODUCT
Lithium Carbonate Extended Release Tablets, USP, 450 mg, 90 and100 count bottles, Rx only, NDC 0143-1277-01, Recall # D-085-2008
CODE
100 count bottle; Lot number 62395C, Exp. Date 3/2008,
90 count bottle; Lot number 62395B, Exp. Date 3/2008
RECALLING FIRM/MANUFACTURER
West-Ward Pharmaceutical Corp, Eatontown, NJ, by letter on December 26, 2007. Firm initiated recall is ongoing.
REASON
Failed USP Dissolution Specification; 18 month stability.
VOLUME OF PRODUCT IN COMMERCE
156 bottles of 100 count.
DISTRIBUTION
Nationwide and PR

Thanks Joanne!

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