FDASeptember 6, 2018drug

Pramipexole dihydrochloride extended release tablets, 0.75 mg, packaged in 30-count bottles, Rx only, Manufactured by: Par Pharmaceutical, Chestnut Ridge, NY 10977, NDC 10370-252-11

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

The hazard

Failed impurities/degradation specifications: Finished product contain a known product impurity about current specification levels.

What to do

FDA enforcement status: Terminated

Brands named

par pharmaceuticalpar

Recall history

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

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Pramipexole dihydrochloride extended release tablets, 0.75 mg, packaged in 30-count bottles, Rx only, Manufactured by: Par Pharmaceutical, Chestnut Ridge, NY 10977, NDC 10370-252-11 — Recall Details · AllClear