October 30, 2019
On September 23, 2019, Sandoz, Inc. announced issued a voluntary recall of all lots of Ranitidine capsules due to an elevated amount of an unexpected impurity (NDMA) found in the active pharmaceutical ingredient.
Express Scripts will mail letters to patients who have received medication impacted by the recall.
The FDA recommends speaking with your prescriber if you want to stop your medication or use an alternative medication.
| Product Name | NDC Number | Lot Nbr. | Expiration Date | Date of Manufacture |
| RANITIDINE 150mg Capsules 500 count | 0781-2855-05 | HD1862 | 04/30/2020 | 04/19/2017 |
| RANITIDINE 150mg Capsules 500 count | 0781-2855-05 | HP9438 | 09/30/2020 | 09/05/2017 |
| RANITIDINE 150mg Capsules 500 count | 0781-2855-05 | HP9439 | 09/30/2020 | 09/06/2017 |
| RANITIDINE 150mg Capsules 500 count | 0781-2855-05 | HP9440 | 09/30/2020 | 09/05/2017 |
| RANITIDINE 150mg Capsules 60 count | 0781-2855-60 | HC9266 | 04/30/2020 | 04/19/2017 |
| RANITIDINE 150mg Capsules 60 count | 0781-2855-60 | HD1865 | 04/30/2020 | 04/19/2017 |
| RANITIDINE 150mg Capsules 60 count | 0781-2855-60 | HP9441 | 09/30/2020 | 09/06/2017 |
| RANITIDINE 150mg Capsules 60 count | 0781-2855-60 | JK7994 | 08/31/2021 | 08/07/2018 |
| RANITIDINE 150mg Capsules 60 count | 0781-2855-60 | JK8659 | 08/31/2021 | 08/07/2018 |
| RANITIDINE 300mg Capsules 30 count | 0781-2865-31 | HD8625 | 04/30/2020 | 04/27/2017 |
| RANITIDINE 300mg Capsules 30 count | 0781-2865-31 | HD9275 | 04/30/2020 | 04/27/2017 |
| RANITIDINE 300mg Capsules 30 count | 0781-2865-31 | HU2207 | 08/31/2020 | 08/24/2017 |
| RANITIDINE 300mg Capsules 30 count | 0781-2865-31 | HX6676 | 03/31/2021 | 03/20/2018 |
| RANITIDINE 300mg Capsules 30 count | 0781-2865-31 | HX6677 | 03/31/2021 | 03/20/2018 |
Additional information is available on the FDA’s website:
Last updated: March 13, 2020