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Class II · ModerateRecall completed

Liothyronine Sodium

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

Does this affect you?
Check your lot numberLot #: DND0058A, Exp. Date 12/2023
Where it was soldNationwide within the United States
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

Failed Impurities/Degradation Specifications.

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 bySun Pharmaceutical Industries Ltd. Survey No. 259/15, Dadra-396 191,(U.T. of D & NH), India foreign manufacturer
Brand nameLIOTHYRONINE SODIUM
Generic nameLIOTHYRONINE SODIUM
Active ingredient(s)LIOTHYRONINE SODIUM
Distributed by / forSun Pharmaceutical Industries, Inc.Cranbury, NJ 08512
NDC62756-589-88
Show the full FDA record
Full product labelLiothyronine Sodium Tablets, USP, 5 mcg, 100-count bottles, Rx only, Distributed by: Sun Pharmaceutical Industries, Inc.Cranbury, NJ 08512, Manufactured by: Sun Pharmaceutical Industries Ltd. Survey No. 259/15, Dadra-396 191,(U.T. of D & NH), India. NDC 62756-589-88
Recalling firmSUN PHARMACEUTICAL INDUSTRIES INC
DistributionNationwide within the United States
Quantity7392 Bottles
Recall initiated2023-10-20
Report date2023-11-08
Recall completed2024-07-25
Recall numberD-0083-2024
ClassificationClass II
FDA statusTerminated
Origin on filePrinceton NJ United States

Related

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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.