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Class II · ModerateRecall completed

Metoprolol Tartrate And Hydrochlorothiazide

Could cause temporary or reversible harm; serious harm is unlikely.

Does this affect you?
Check your lot number2005005745
Where it was soldFL, GA, SC
Find the lot number printed on your box or bottle. If it matches — and you take this medicine — call your pharmacist. Don't stop a prescribed medicine on your own.

What happened

CGMP Deviations: Intermittent exposure to temperature excursion during storage.

What to do

  1. Check the lot number and expiry on your medicine against the recall above.
  2. Talk to your pharmacist or doctor before changing anything — don't stop on your own.
  3. Report any problems to FDA MedWatch (1-800-FDA-1088 or fda.gov/medwatch).

Who makes it

Made byAlembic Pharmaceuticals Inc.
Brand nameMETOPROLOL TARTRATE AND HYDROCHLOROTHIAZIDE
Generic nameMETOPROLOL TARTRATE AND HYDROCHLOROTHIAZIDE
Active ingredient(s)HYDROCHLOROTHIAZIDE, METOPROLOL TARTRATE
Distributed by / forAlembic Pharmaceuticals, Inc. 750 Route 202, Bridgewater, NJ 08807 USA
NDC62332-115-31
Show the full FDA record
Full product labelMetoprolol Tartrate and Hydrochlorothiazide Tablets, USP 50 mg/25 mg 100 Tablets Rx only NDC 62332-115-31 Manufactured for: Alembic Pharmaceuticals, Inc. 750 Route 202, Bridgewater, NJ 08807 USA
Recalling firmCardinal Health Inc.
DistributionFL, GA, SC
Quantity71 bottles
Recall initiated2021-03-15
Report date2021-06-02
Recall completed2024-06-17
Recall numberD-0412-2021
ClassificationClass II
FDA statusTerminated
Origin on fileDublin OH United States

Related

Hydrochlorothiazide recallsMetoprolol recallsRecent drug recallsCheck another medication

Source: U.S. FDA enforcement database (openFDA). Look this up on the official FDA recalls site ↗

This is public FDA recall information, not medical advice. A recall does not always mean your specific bottle is affected. Never stop a prescribed medicine without asking your pharmacist or doctor.