Reported Jun 8, 2022 · Terminated

Losartan Potassium Tablets, USP, 100 mg, Rx Only, Manufactured by: Vivimed Life Sciences Private Limited, Plot No.,…

Strides Pharma Inc.

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: Strides Pharma Inc. · 2 Tower Center Blvd Ste 1102 · East Brunswick, NJ · 08816-1100

Is this the product you have?

  • Losartan Potassium Tablets, USP, 100 mg, Rx Only
  • Manufactured byVivimed Life Sciences Private Limited, Plot No., 101, 102, 107 & 108, SIDCO Pharmaceutical Complex, Alathur, Kanchipuram - 603 110, Tamilnadu, India
  • Distributed byStrides Pharma Inc., East Brunswick, NJ 08816. 90 film coated tablets NDC 64380-935-05 1000 film coated tablets NDC 64380-935-08
Lot codes and dates

9 of 9 products

Products covered by this recall
#Product as published
164380-935-05 Lots 7901047B, 7901048B, 7901049B & 7901050B, Exp Date Jul-22
2Lots 7901185A, 7901186A, 7901187A & 7901188A, Exp Date Oct-22
3Lots 7901250A, 7901251A & 7901252A, Exp Date Nov-22. 64380-935-08 Lots 7900813B, 7900814B, 7900908A, 7900935A, 7900936A, 7900937A, 7900938A & 7900939B, Exp Date May-22
4Lots 7901043A, 7901044A, 7901045A & 7901046A, Exp Date Jul-22
5Lots 7901158B, 7901159B, 7901160B, 7901161A, 7901182A & 7901183A, Exp Date Sep-22
6Lots 7901184A, 7901189A, 7901190A, 7901191A, 7901192A, 7901193A, 7901194A & 7901195A, Exp Date Oct-22
7Lots 7901295B, 7901296B, 7901297B, 7901298B, 7901299B, 7901300B, 7901301B & 7901302B, Exp Date Nov-22
8Lots 7901338A, 7901339A, 7901340A, 7901341A & 7901342A, Exp Date Dec-22
9Lot 7901387A, Exp Date Jan-23
Amount recalled
96966 bottles

This recall covers 3 products

The agency filed one notice per product. You are reading one of them; the other 2 are below.

Where it was sold

  • Nationwide

Why it was recalled

CGMP Deviations- AZIDO Impurity levels observed to be above acceptable limits

This product could cause temporary or reversible health problems — stop using it.

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The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.

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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA drug enforcement) notice

Notice updated Oct 20, 2023 · Data as of Sep 19, 5:07 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.