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FDADecember 20, 2019drug

Ranitidine Tablets, USP 150 mg , a). 4 count bottle (NDC 70934-017-04), b). 20-count bottle (NDC 70934-017-20), c). 24-count bottle (NDC 70934-017-24) d). 30-count bottle (NDC 70934-017-30) e). 90-count bottle (NDC 70934-017-90), Rx Only, Repackaged by: Northwind Pharmaceuticals North Brenheim, N...

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

The hazard

CGMP Deviations: Presence of NDMA impurity detected in product.

What to do

FDA enforcement status: Terminated

Brands named

denton pharmadenton

Recall history

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

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Ranitidine Tablets, USP 150 mg , a). 4 count bottle (NDC 70934-017-04), b). 20-count bottle (NDC 70934-017-20), c). 24-count bottle (NDC 70934-017-24) d). 30-count bottle (NDC 70934-017-30) e). 90-count bottle (NDC 70934-017-90), Rx Only, Repackaged by: Northwind Pharmaceuticals North Brenheim, N... — Recall Details · AllClear