FDADecember 20, 2023drug

Desloratadine Tablets USP 5mg a) 100 count (NDC 68180-153-01) and b) 500 count (NDC 68180-153-02) bottles, Rx Only, Manufactured for: Lupin Pharmaceuticals, Inc. Baltimore, Maryland 21202.

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

The hazard

CGMP Deviations: N-Nitroso Desloratadine impurity result exceeded the acceptable intake limit.

What to do

FDA enforcement status: Terminated

Brands named

lupin pharmaceuticalslupin

Recall history

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

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