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3/31/04 at 5:02pm
Thread Starter 
The FDA has released the following information.

PRODUCT
PREMARIN (conjugated estrogens tablets, USP), 0.625 mg, 1000 count bottles, Rx only. Recall # D-130-4.

CODE
Lot Number/Expiration Date: A57921 (October 2005).

RECALLING FIRM/MANUFACTURER
Richmond Division of Wyeth, Richmond, VA, by letter dated on 3/10/2004. Firm initiated recall is ongoing.

REASON
Dissolution Failure.

VOLUME OF PRODUCT IN COMMERCE
48 bottles.

DISTRIBUTION
Nationwide.
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