NDC 68180-210

Losartan Potassium 25 mg tablet

On the label: Lupin Pharmaceuticals, Inc..

Where it's made

Recalls

• Mar 31, 2022 · Class II · Lupin Pharmaceuticals Inc.
  CGMP Deviations- AZIDO Impurity levels observed to be above acceptable limits
  Lots: H001333, exp. date Nov-22 H002786, exp. date Jan-23 H101282, exp. date Feb-23 H001189, exp. date Nov-22 H002955, exp. date Jan-23 H101285, exp. date Feb-23 H001714, exp. date Dec-22 H000523, exp. date Jan-23 H101989, exp. date Mar-23 H001940, exp. date Dec-22 H003080, exp. date Jan-23 H1…
• Mar 31, 2022 · Class II · Lupin Pharmaceuticals Inc.
  CGMP Deviations- AZIDO Impurity levels observed to be above acceptable limits
  Lots: H903720, exp. date Oct-22 H001876, exp. date Dec-22 H003002, exp. date Jan-23 H903774, exp. date Oct-22 H001877, exp. date Dec-22 H003003, exp. date Feb-23 H000849, exp. date Nov-22 H002127, exp. date Dec-22 H003004, exp. date Feb-23 H001412, exp. date Nov-22 H002128, exp. date Dec-22 H0…
• Mar 31, 2022 · Class II · Lupin Pharmaceuticals Inc.
  CGMP Deviations- AZIDO Impurity levels observed to be above acceptable limits
  Lots: H903573, exp. date Oct-22 H002311, exp. date Dec-22 H100713, exp. date Mar-23 H001060, exp. date Nov-22 H002620, exp. date Jan-23 H100714, exp. date Mar-23 H001456, exp. date Nov-22 H002313, exp. date Jan-23 H100934, exp. date Mar-23 H001457, exp. date Nov-22 H002490, exp. date Jan-23 H1…

Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.

Product details

Generic drug

Losartan: every company that makes it

Form

tablet, oral

Strength

25 mg

Approval

ANDA ANDA078232

On the market since

Oct 6, 2010

Package NDCs

68180-210-01 68180-210-03 68180-210-06 68180-210-09

Official label

DailyMed (National Library of Medicine), updated Jun 30, 2026

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