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Class III · Lower riskRecall completed

Telmisartan and Hydrochlorothiazide Tablets

Unlikely to cause harm — often a labeling or packaging issue.

Does this affect you?
Check your lot numberBatch: BZ74G001 Exp. 12/2021.
Where it was soldNationwide USA
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

Superpotent; Hydrochlorothiazide

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 byTorrent Pharmaceuticals LTD., Indrad-382 721, India. Manufactured for: Torrent Pharma Inc., Basking Ridge, NJ 07920 foreign manufacturer
Distributed by / forTorrent Pharma Inc., Basking Ridge, NJ 07920
NDC13668-159-30
Show the full FDA record
Full product labelTelmisartan and Hydrochlorothiazide Tablets, USP, 40 mg/12.5 mg, 30 count bottles, Rx only, Manufactured by: Torrent Pharmaceuticals LTD., Indrad-382 721, India. Manufactured for: Torrent Pharma Inc., Basking Ridge, NJ 07920. NDC: 13668-159-30
Recalling firmTorrent Pharma Inc.
DistributionNationwide USA
Quantity27,312 Bottles
Recall initiated2021-12-01
Report date2021-12-22
Recall completed2024-05-12
Recall numberD-0285-2022
ClassificationClass III
FDA statusTerminated
Origin on fileBasking Ridge NJ United States

Related

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.