NDC 51655-418

LOSARTAN POTASSIUM50 mg 50 mg tablet, film coated

On the label: Northwind Pharmaceuticals. It's a repackaged product: Northwind Pharmaceuticals rebottles it from Strides Pharma Science Limited's NDC 64380-934.

Where the pills inside were made

Strides Pharma Science Limited

Chengalpattu, India · makes it, tests it and packages it

Problems found, fixed voluntarily Last FDA inspection Apr 5, 2024. 7 inspections on record.

Repackaging site

• Northwind Health Company, LLC, Indianapolis, IN, United States · repackages it

Recalls

• Jun 26, 2023 · Class II · Terminated
  Presence of Foreign Substance: Presence of a small piece of blue plastic embedded in the tablet.
  Lots: Lot#: 7901903A, exp. date 04/2024
• May 18, 2022 · Class II · Terminated
  CGMP Deviations- AZIDO Impurity levels observed to be above acceptable limits
  Lots: NDC 64380-933-05 Lot 7901007A, Exp Date Jun-22; Lot 7901144A, 7901178A & 7901179A, Exp Date Sep-22; Lots 7901246A & 7901247A, Exp Date Oct-22; Lot 7901343A, Exp Date Dec-22. NDC 64380-933-08 Lot 7901006A, Exp Date Jun-22; Lot 7901145A & 7901180A, Exp Date Sep-22; Lot 7901181A, Exp Date Oct-22.
• May 18, 2022 · Class II · Terminated
  CGMP Deviations- AZIDO Impurity levels observed to be above acceptable limits
  Lots: NDC 64380-934-05 Lot 7901146A, 7901147A, 7901148A & 7901149A, Exp Date Sep-22; Lot 7901279A, 7901280A, 7901281A, 7901282A, 7901283A & 7901284A, Exp Date Nov-22; Lot 7901359A, 7901360A & 7901361A, Exp Date Dec-22; Lot 7901362A, 7901406A, 7901407A, 7901408A & 7901409A, Exp Date Jan-23. 64380-934-0…
• May 18, 2022 · Class II · Terminated
  CGMP Deviations- AZIDO Impurity levels observed to be above acceptable limits
  Lots: 64380-935-05 Lots 7901047B, 7901048B, 7901049B & 7901050B, Exp Date Jul-22; Lots 7901185A, 7901186A, 7901187A & 7901188A, Exp Date Oct-22; Lots 7901250A, 7901251A & 7901252A, Exp Date Nov-22. 64380-935-08 Lots 7900813B, 7900814B, 7900908A, 7900935A, 7900936A, 7900937A, 7900938A & 7900939…

Product details

Generic drug

Losartan: see every company that makes it

Form

tablet, film coated, oral

Strength

50 mg

Approval

ANDA ANDA090382

On the market since

Jul 15, 2020

Package NDCs

51655-418-26

Official label

DailyMed (National Library of Medicine), updated Jan 1, 2026

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