Product Detail

Product Description Prempro (Conjugated Estrogen/Medroxyprogesterone Acetate) tablets 0.625 mg/5.0 mg, 1 blister card containing 28 tablets, Rx only, Wyeth Pharmaceuticals Inc., Philadelphia, PA 1910, NDC 0046-0875-11

Recall Number D-631-2013

Classification Class III

Code Info Lots: E77055, E96153, & F11111 Exp: 06/13

Product Distributed Qty 135,520 blister cards

Reason For Recall Failed Dissolution Specifications: Pfizer Inc. (Pfizer) is recalling PREMPRO (conjugated estrogens/medroxyprogesterone acetate tablets) because certain lots for this product may not meet the specification for conjugated estrogens dissolution.

Event Detail

Event Id 65393

Product Type Drugs

Status Ongoing

Recalling Firm
Pfizer Inc.
City New York

State NY
Country US

Voluntary / Mandated Voluntary: Firm Initiated

Recall Initiation Date 2013-05-31

Initial Firm Notification of Consignee or Public Letter

Distribution Pattern Nationwide and Puerto Rico