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Class II · ModerateRecall completed

Prednisone

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

Does this affect you?
Check your lot numberLot #: 7248988B, Exp 9/2023
Where it was soldUS Nationwide
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

Presence of foreign tablet: 2.5 mg tablet in a 20 mg bottle of Prednisone Tablets

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 byStrides Pharma Science Ltd., Bengaluru - 562106, India, Distributed by: Strides Pharma Inc., East Brunswick, NJ 08816 foreign manufacturer
Brand namePREDNISONE
Generic namePREDNISONE
Active ingredient(s)PREDNISONE
Distributed by / forStrides Pharma Inc., East Brunswick, NJ 08816
NDC64380-785-06
Show the full FDA record
Full product labelPrednisone Tablets USP, 20 mg, 100-count bottle, Rx Only, Manufactured by: Strides Pharma Science Ltd., Bengaluru - 562106, India, Distributed by: Strides Pharma Inc., East Brunswick, NJ 08816, NDC 64380-785-06.
Recalling firmStrides Pharma Inc.
DistributionUS Nationwide
Quantity1032 bottles
Recall initiated2022-07-19
Report date2022-08-17
Recall completed2023-06-21
Recall numberD-1330-2022
ClassificationClass II
FDA statusTerminated
Origin on fileEast Brunswick 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.