US Drug Recall Register
Class III · Low risk Terminated Initiated Apr 21, 2021 (5 years ago)

Acyclovir Tablets, USP, 400 mg, 100 Tablets, Rx Only, Distributed by: Avet…

Class III — Low risk. Unlikely to cause harm, but violates FDA regulations.

Why it was recalled

Labeling: Incorrect or Missing Lot and/or Exp Date

What was recalled

Acyclovir Tablets, USP, 400 mg, 100 Tablets, Rx Only, Distributed by: Avet Pharmaceuticals Inc., East Brunswick, NJ 08816, NDC 23155-227-01. Packaged in 150 cc white HDPE bottle

Recalling firm
Heritage Pharmaceuticals Inc
NDC code
23155-227-01
Origin
NJ, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0367-2021

What should you do? A recall doesn't always mean your specific bottle is affected - it often applies to certain lots only. Check the lot number on your package against the FDA notice, and talk to your pharmacist before stopping any medication.

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