FDANovember 6, 2019drug

Aurobindo Ranitidine Capsules 150 mg, 500 count bottle, Rx Only Distributed by: Aurobindo Pharma USA, Inc. 279 Princeton-Hightstown Road East Windsor, NJ 08520 NDC 59651-144-05

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

CGMP Deviations: N-nitrosodimethylamine (NDMA) has been detected in Ranitidine tablets, capsules and syrups.

What to do

FDA enforcement status: Ongoing

Brands named

auromedics pharmaauromedics

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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Aurobindo Ranitidine Capsules 150 mg, 500 count bottle, Rx Only Distributed by: Aurobindo Pharma USA, Inc. 279 Princeton-Hightstown Road East Windsor, NJ 08520 NDC 59651-144-05 — Recall Details · AllClear