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Lucid Pharma Recalls

1 recall on record · June 28, 2017 to June 28, 2017 · Drugs

June 28, 2017DrugsFDA

Lucid Pharma LLC recalls Venlafaxine Hydrochloride Extended-Release Capsules USP, 75 mg, packaged in a) 30-count bottles (NDC 52343-132-30) and b

Hazard: Failed Tablet/Capsules Specifications: pharmacists complaints for bottles containing melted capsules.

Lucid Pharma Recalls | RecallWatchUSA