Triamterene and Hydrochlorothiazide Tablets recall: Subpotent
Triamterene and Hydrochlorothiazide Tablets, USP 37.5 mg/25 mg, 100-count bottle, Rx only, Mylan Pharmaceuticals, Inc. Morgantown, WV 26505, NDC…
Why was Triamterene and Hydrochlorothiazide Tablets recalled?
Subpotent Drug
What should I do if I have this product?
Review the official FDA enforcement record for current instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
Lot #: 2007979, Exp. 11/30/2020
- Product
- Triamterene and Hydrochlorothiazide Tablets, USP 37.5 mg/25 mg, 100-count bottle, Rx only, Mylan Pharmaceuticals, Inc. Morgantown, WV 26505, NDC…
- Recalling firm
- Mylan Pharmaceuticals Inc.
- Quantity
- 28,436 bottles
- Distribution
- Nationwide within the United States
- Recall date
- July 18, 2018
- Classification
- Class III
- Status
- Terminated
- Agency
- FDA (drug)