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FDA (Drug enforcement)Recalled 2022-03-31closedclass ii

Lupin Pharmaceuticals Inc.: Losartan Potassium Tablets USP, 100 mg, a) 90-count bottles (NDC# 68180-378-03), b) 1000-count bottles (NDC# 68180-378-09), Rx Only, Manufactured By: Lupin Limited, Pithamp

Is my product affected?

Losartan Potassium Tablets USP, 100 mg, a) 90-count bottles (NDC# 68180-378-03), b) 1000-count bottles (NDC# 68180-378-09), Rx Only, Manufactured By: Lupin Limited, Pithampur, India, MFG For: Lupin Pharmaceuticals, Inc. Baltimore, Maryland 21202, USA.

  • Brand LOSARTAN POTASSIUM

Check against the official notice below — it lists the full affected range.

What happened

Lupin Pharmaceuticals Inc. is recalling Losartan Potassium Tablets USP, 100 mg in two bottle sizes (90-count bottles with NDC# 68180-378-03 and 1000-count bottles with NDC# 68180-378-09) due to CGMP deviations with AZIDO impurity levels observed above acceptable limits. The recalled product was manufactured by Lupin Limited and distributed nationwide, with a total of 1,247,067 bottles affected across multiple lot codes with expiration dates ranging from October 2022 through March 2023.

The recall record does not specify a remedy or what consumers should do with recalled product.

Written by software from the official notice below. Not reviewed by a lawyer.

Hazard

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

Details from the source

Reason for recall: CGMP Deviations- AZIDO Impurity levels observed to be above acceptable limits Distribution: Product was distributed nationwide Quantity: 1,247,067 bottles Lot/code info: 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 H100935, exp. date Mar-23 H001470,, exp. date Nov-22 H002842, exp. date Jan-23 H101081, exp. date Mar-23 H001484, exp. date Dec-22 H002843, exp. date Jan-23 H101148, exp. date Mar-23 H001485, exp. date Dec-22 H002995, exp. date Jan-23 H101639, exp. date Mar-23 H001708, exp. date Dec-22 H003199, exp. date Feb-23 H101480, exp. date Mar-23 H002314, exp. date Dec-22 H003200, exp. date Feb-23 H101822, exp. date Mar-23 H001709, exp. date Dec-22 H100028, exp. date Feb-23 H101481, exp. date Mar-23 H002001, exp. date Dec-22 H100712, exp. date Feb-23 H102288, exp. date Mar-23 H001991, exp. date Dec-22 H100221, exp. date Feb-23 H002000, exp. date Dec-22 H100222, exp. dateFeb-23 H903582, exp. date Oct-22 H001707, exp. dateDec-22 H100220, exp. date Feb-23 H000556,, exp. date Nov-22 H003045, exp. date Dec-22 H100901, exp. date Mar-23 H000557, exp. date Nov-22 H002391, exp. date Dec-22 H101078, exp. date Mar-23 H001061, exp. date Nov-22 H002312, exp. date Jan-23 H101479, exp. date Mar-23 H001062, exp. date Nov-22 H002517, exp. date Jan-23 H101496, exp. date Mar-23 H001431, exp. date Nov-22 H002841, exp. date Jan-23 H101821, exp. date Mar-23 H002341, exp. date Nov-22 H003044, exp. date Feb-23 H102286, exp. date

Source

Official record: FDA (Drug enforcement) ↗

Republished from the official source above; details can change — the source record controls.

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