Ranitidine capsule recall- Sandoz Inc.

Tue, 09/24/2019 - 14:33

On September 23, 2019, Sandoz, Inc. announced a voluntary recall of Ranitidine 150mg capsules, and 300mg capsules due to an elevated amount of an unexpected impurity (NDMA) found in the active pharmaceutical ingredient.

The FDA recommends patients to continue to take their medication and speak to their physician or pharmacist on alternate healthcare treatment options.

Product Name

NDC Number

Lot Nbr.

Expiration Date

Date Of Manufacture

RANITIDINE 150mg Capsules 500 count

0781-2855-05

HD1862

4/30/2020

4/19/2017

RANITIDINE 150mg Capsules 500 count

0781-2855-05

HP9438

9/30/2020

9/5/2017

RANITIDINE 150mg Capsules 500 count

0781-2855-05

HP9439

9/30/2020

9/6/2017

RANITIDINE 150mg Capsules 500 count

0781-2855-05

HP9440

9/30/2020

9/5/2017

RANITIDINE 150mg Capsules 60 count

0781-2855-60

HC9266

4/30/2020

4/19/2017

RANITIDINE 150mg Capsules 60 count

0781-2855-60

HD1865

4/30/2020

4/19/2017

RANITIDINE 150mg Capsules 60 count

0781-2855-60

HP9441

9/30/2020

9/6/2017

RANITIDINE 150mg Capsules 60 count

0781-2855-60

JK7994

8/31/2021

8/7/2018

RANITIDINE 150mg Capsules 60 count

0781-2855-60

JK8659

8/31/2021

8/7/2018

RANITIDINE 300mg Capsules 30 count

0781-2865-31

HD8625

4/30/2020

4/27/2017

RANITIDINE 300mg Capsules 30 count

0781-2865-31

HD9275

4/30/2020

4/27/2017

RANITIDINE 300mg Capsules 30 count

0781-2865-31

HU2207

8/31/2020

8/24/2017

RANITIDINE 300mg Capsules 30 count

0781-2865-31

HX6676

3/31/2021

3/20/2018

RANITIDINE 300mg Capsules 30 count

0781-2865-31

HX6677

3/31/2021

3/20/2018

Additional information is available on the FDA's website.

Last updated: Tue, 10/08/2019 - 14:27

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