FDAApril 30, 2019drug

Mycophenolate Mofetil for Injection, USP 500 mg, 4 Single Dose Vials, Rx Only, Distributed by: Par Pharmaceutical Chestnut Ridge, NY 10977 NDC 342023-172-044

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

The hazard

Presence of Particulate Matter; glass fragment observed in one vial of reconstituted product

What to do

FDA enforcement status: Terminated

Brands named

par pharmaceuticalpar

UPCs

342023172044

Recall history

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

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Mycophenolate Mofetil for Injection, USP 500 mg, 4 Single Dose Vials, Rx Only, Distributed by: Par Pharmaceutical Chestnut Ridge, NY 10977 NDC 342023-172-044 — Recall Details · AllClear