Sandoz Incorporated recalls Fluoxetine Capsules USP, 20 mg, 100 count bottle, Rx Only, 100 Capsules, Sandoz Inc Princeton, NJ 08540 NDC 0781-2822-01
Recalled December 17, 2014 · FDA recall D-0291-2015 · Sandoz Incorporated
Hazard
Labeling: Illegible Label: Sandoz Inc. is recalling of one lot of Fluoxetine Capsules due to an illegible logo on the capsule. · FDA Class III
Units
1,008 bottles
Sold at
AZ
Description
Labeling: Illegible Label: Sandoz Inc. is recalling of one lot of Fluoxetine Capsules due to an illegible logo on the capsule.
Product
Fluoxetine Capsules USP, 20 mg, 100 count bottle, Rx Only, 100 Capsules, Sandoz Inc Princeton, NJ 08540 NDC 0781-2822-01
Manufacturer(s)
Sandoz Incorporated
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →