Mylan Pharmaceuticals Inc. recalls PrednisoLONE Sodium Phosphate Orally Disintegrating Tablets 15 mg, Rx Only, 48-count bottle, NDC 00378-4715-22
Recalled May 30, 2018 · FDA recall D-0830-2018 · Mylan Pharmaceuticals
Hazard
CGMP Deviations · FDA Class II
Units
9,906 48-count bottles
Sold at
Recalling firm distributed product to wholesalers throughout the United States, including Puerto Rico.
Description
CGMP Deviations
Product
PrednisoLONE Sodium Phosphate Orally Disintegrating Tablets 15 mg, Rx Only, 48-count bottle, NDC 00378-4715-22
Manufacturer(s)
Mylan Pharmaceuticals Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →