RecallRadar

FDA Drug recall D-0367-2021

Acyclovir Tablets, USP, 400 mg, 100 Tablets, Rx Only, Distributed by: Avet Pharmaceuticals Inc., East Brunswick, NJ 08816, NDC 23155-227-01

On 2021-05-12 the FDA classified a Class III recall of Acyclovir Tablets, USP, 400 mg, 100 Tablets, Rx Only, Distributed by: Avet Pharmaceuticals Inc., East Brunswick, NJ 08816, NDC 23155-227-01 by Heritage Pharmaceuticals, citing labeling: Incorrect or Missing Lot and/or Exp Date.

Read the official FDA Drug notice

AgencyFDA Drug
Recall numberD-0367-2021
ClassificationClass III
Statusterminated
Initiated2021-04-21
Published2021-05-12
Last updated2026-09-13 11:52 UTC
CompanyHeritage Pharmaceuticals
DistributionOH

Product

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

Reason

Labeling: Incorrect or Missing Lot and/or Exp Date

Identifiers

ndc23155-227-01
ndc23155-227-05
ndc23155-228-01
ndc23155-228-05
code_infoLot A120036, Exp DEC 2023

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:52 UTC. Current status: terminated.

Source

Official record: https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0367-2021%22

RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.