Triamterene and Hydrochlorothiazide Tablets, USP 37.5 mg/25 mg, 100-count bottle, Rx only, Mylan Pharmaceuticals, Inc. Morgantown, WV 26505, NDC 0378-1352-01
Reported: July 18, 2018 Initiated: July 9, 2018 #D-0978-2018
Product Description
Triamterene and Hydrochlorothiazide Tablets, USP 37.5 mg/25 mg, 100-count bottle, Rx only, Mylan Pharmaceuticals, Inc. Morgantown, WV 26505, NDC 0378-1352-01
Reason for Recall
Subpotent Drug
Details
- Recalling Firm
- Mylan Pharmaceuticals Inc.
- Units Affected
- 28,436 bottles
- Distribution
- Nationwide within the United States
- Location
- Morgantown, WV
Frequently Asked Questions
What product was recalled? ▼
Triamterene and Hydrochlorothiazide Tablets, USP 37.5 mg/25 mg, 100-count bottle, Rx only, Mylan Pharmaceuticals, Inc. Morgantown, WV 26505, NDC 0378-1352-01. Recalled by Mylan Pharmaceuticals Inc.. Units affected: 28,436 bottles.
Why was this product recalled? ▼
Subpotent Drug
Which agency issued this recall? ▼
This recall was issued by the FDA Drug on July 18, 2018. Severity: Low. Recall number: D-0978-2018.
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