FDADecember 4, 2017drug

Viokace (pancrelipase) tablets, 20,880 USP units, 100-count bottle, Rx only, Distributed by; Allergan USA Inc., Irvine, CA 92612, Manufactured in Canada, NDC 58914-117-10

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

The hazard

Subpotent Drug: One lot of Viokace is being recalled since product stability testing results did not meet the specifications for enzyme profile.

What to do

FDA enforcement status: Terminated

Brands named

allergan

Recall history

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

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Viokace (pancrelipase) tablets, 20,880 USP units, 100-count bottle, Rx only, Distributed by; Allergan USA Inc., Irvine, CA 92612, Manufactured in Canada, NDC 58914-117-10 — Recall Details · AllClear