FDAJune 1, 2017drug

Venlafaxine Hydrochloride Extended-Release Capsules USP, 75 mg, packaged in a) 30-count bottles (NDC 52343-132-30) and b) 90-count bottles (NDC 52343-132-90), Rx only, Distributed by: Lucid Pharma LLC, 2 Tower Center Blvd, Suite-1101-B, East Brunswick, NJ 08816 USA.

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

The hazard

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

What to do

FDA enforcement status: Terminated

Brands named

lucid pharmalucid

Recall history

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

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Venlafaxine Hydrochloride Extended-Release Capsules USP, 75 mg, packaged in a) 30-count bottles (NDC 52343-132-30) and b) 90-count bottles (NDC 52343-132-90), Rx only, Distributed by: Lucid Pharma LLC, 2 Tower Center Blvd, Suite-1101-B, East Brunswick, NJ 08816 USA. — Recall Details · AllClear