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FDAFDA · Food and drugs·Recall number D-0492-2017

Mirtazapine Tablets, USP 45 mg, a) 30 count, b) 100 count and c) 500 count bottles, Rx only, Mylan Pharmaceuticals Inc., Morgantown, WV

Published March 15, 2017 · Recall initiated: January 19, 2017

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

Presence of Foreign Tablets/Capsules; possibility of Glipizide 10 mg tablet in bottle

What to do

Voluntary: Firm initiated · E-Mail

Recall details

Brand
MIRTAZAPINE
Manufacturer
Mylan Pharmaceuticals Inc.
Distributor
Nationwide
UPC
0303783545936
Lot
a) 3078937 and 3078938 (NDC 0378-3545-93), exp August 2019 b) 3078937 (NDC 0378-3545-01), exp August 2019 c) 3078936 (0378-3545-05), exp August 2019
Risk classification
Class II
Area (FDA)
drug
Country
United States

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