In Brief: Ranitidine Returns

The FDA has approved a new tablet formulation of the H2-receptor antagonist (H2RA) ranitidine from one manufacturer (VKT Pharma/Rising Pharma). It is only available by prescription. In 2020, the FDA requested that all formulations of ranitidine be withdrawn from the market because unacceptable levels of the nitrosamine compound N-nitrosodimethylamine (NDMA), a potentially carcinogenic contaminant, had been detected in ranitidine samples.

Publication Details

Journal
˜The œmedical letter on drugs and therapeutics/˜The œmedical letter
Published
2026-04-13
DOI
https://doi.org/10.58347/tml.2026.1752e
Primary Topic
Tuberculosis Research and Epidemiology
Type
article
Field-Weighted Citation Impact
0.00
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article

In Brief: Ranitidine Returns

˜The œmedical letter on drugs and therapeutics/˜The œmedical letter
Tuberculosis Research and Epidemiology
article

In Brief: Ranitidine Returns

article en

Abstract

The FDA has approved a new tablet formulation of the H2-receptor antagonist (H2RA) ranitidine from one manufacturer (VKT Pharma/Rising Pharma). It is only available by prescription. In 2020, the FDA requested that all formulations of ranitidine be withdrawn from the market because unacceptable levels of the nitrosamine compound N-nitrosodimethylamine (NDMA), a potentially carcinogenic contaminant, had been detected in ranitidine samples.

˜The œmedical letter on drugs and therapeutics/˜The œmedical letterVol. 68(1752)
Openalex Percentile: Top 15%
Tuberculosis Research and Epidemiology
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In Brief: Ranitidine Returns · ˜The œmedical letter on drugs and therapeutics/˜The œmedical letter (2026) | TGRS Research Map | TGRS