CLASS II ONGOING Drug recall · Reported 24 Sep 2025 · FDA Enforcement Report

Entecavir Tablets, USP, 5 mg recalled by Zydus Pharmaceuticals (USA)

Zydus Pharmaceuticals (USA) is recalling Entecavir Tablets, USP, 5 mg, distributed nationwide in the US. The recall was initiated on 4 Sep 2025 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesLot E309376; Exp 11/30/2025
NDC68382-920, 68382-921
Quantity recalled4344 bottles

Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.

Recall details

Recall number
D-0656-2025
FDA event ID
97556
Recalling firm
Zydus Pharmaceuticals (USA), Pennington, NJ
Manufacturer
Zydus Pharmaceuticals USA Inc.
Classification
Class II
Status
Ongoing
Recall initiated
4 Sep 2025
FDA classified
18 Sep 2025
Reported
24 Sep 2025
Type
Voluntary: Firm initiated
Customers notified by
N/A
Reason category
Potency & Assay

Timeline

4 Sep 2025Recall initiated by company
18 Sep 2025Classified by FDA+14 days
24 Sep 2025Published in enforcement report+6 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

Failed Impurity/Degradation Specifications

Potency and specification recalls happen when a batch tests outside its approved limits for strength, purity or dissolution, which can mean the dose delivered is higher or lower than labelled.

Product as listed by the FDA

Entecavir Tablets, USP, 0.5 mg, 30 Tablets, Rx Only, Manufactured by: Zydus Lifesciences Ltd., Ahmedabad, India, Distributed by: Zydus Pharmaceuticals (USA) Inc., Pennington, NJ 08534, NDC 68382-920-06.

Where it was distributed

U.S. Nationwide

Nationwide

Questions about this recall

Is Entecavir Tablets, USP, 5 mg recalled?

Yes. Zydus Pharmaceuticals (USA) recalled Entecavir Tablets, USP, 5 mg on 4 Sep 2025. The recall is Class II and its status is Ongoing. Recall number D-0656-2025.

Why was it recalled?

Failed Impurity/Degradation Specifications

Which lots are affected?

Lot E309376; Exp 11/30/2025

Where was it sold?

U.S. Nationwide

What should I do if I have it?

Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.

What does Class II mean?

Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.

Read the official FDA notice · Source record retrieved 21 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

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