WhichRecall
Class IIReported 2025-04-16

Voriconazole Tablets 200 mg, 30-count bottle, Rx Only, Manufactured by: Glenmark Pharmaceuticals Limited, Pithampur, Madhya Pradesh 454775, India, Manufactured for: Glenmark Pharmaceuticals Inc. USA, Mahwah, NJ 07430. NDC# 68462-573-30

Recalled by Glenmark Pharmaceuticals Inc., USA

Reason for Recall

CGMP Deviations

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Recall Number
D-0318-2025
Classification
Class II
Status
Ongoing
Category
drug
Initiated
2025-03-13
Reported
2025-04-16
Distribution
U.S. Nationwide
Code Info
Lot # 17230853, exp. date Mar-25 17231271, exp. date May-25 17231300, exp. date May-25 17242050, exp. date Oct-26 17231046, exp. date Apr-25 17241156, exp. date Jun-26 17241388, exp. date Jul-26 17241800, exp. date Sep-26
Source: openFDA enforcement report. WhichRecall is not affiliated with the FDA. See our disclaimer.
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