FDAFDA · Food and drugs·Recall number D-0831-2018
PrednisoLONE Sodium Phosphate Orally Disintegrating Tablets, 30 mg, Rx Only, 48-count bottle, NDC 00378-4730-22
Published May 30, 2018 · Recall initiated: April 30, 2018
Status when published: Terminated — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
CGMP Deviations
What to do
Voluntary: Firm initiated · Letter
Recall details
- Manufacturer
- Mylan Pharmaceuticals Inc.
- Distributor
- Recalling firm distributed product to wholesalers throughout the United States, including Puerto Rico.
- Lot
- Lot #: 3082921; Exp. 12/18 3088975; Exp. 06/19
- Risk classification
- Class II
- Area (FDA)
- drug
- Country
- United States
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