Alara Pharmaceutical Co recalls Levothyroxine Sodium Tablets, USP, 175 mcg in 90 ct bottles, Manufactured by Patheon Puerto Rico Inc., for Alara Pharmac
Recalled January 2, 2013 · FDA recall D-104-2013 · Alara Pharmaceutical
Hazard
Subpotent; 15 month stability · FDA Class II
Units
7,432 bottles
Sold at
Nationwide
Description
Subpotent; 15 month stability
Product
Levothyroxine Sodium Tablets, USP, 175 mcg in 90 ct bottles, Manufactured by Patheon Puerto Rico Inc., for Alara Pharmaceutical Corp, San Juan, PR
Manufacturer(s)
Alara Pharmaceutical Co
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →