CLASS III Drug recall · Reported 11 Oct 2023 · FDA Enforcement Report

HydrALAZINE Hydrochloride Tablets, USP, 10 mg (10 recalled

Amerisource Health Services is recalling HydrALAZINE Hydrochloride Tablets, USP, 10 mg (10 x per, distributed nationwide in the US. The recall was initiated on 1 Sep 2023 and the FDA has classified it as Class III.

Check your package

Lot, batch or date codesLot#: 1007002, Exp 12/31/2023
Quantity recalled3,344 cartons

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-0039-2024
FDA event ID
93089
Recalling firm
Amerisource Health Services, Columbus, OH
Classification
Class III
Status
Terminated
Recall initiated
1 Sep 2023
FDA classified
5 Oct 2023
Reported
11 Oct 2023
Type
Voluntary: Firm initiated
Customers notified by
Letter
Reason category
Potency & Assay

Timeline

1 Sep 2023Recall initiated by company
5 Oct 2023Classified by FDA+34 days
11 Oct 2023Published 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 Impurities/Degradation Specifications: Out of Specification results in the repackaged product for impurities at the 12-month time point.

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

HydrALAZINE Hydrochloride Tablets, USP, 10 mg, 100 Tablets (10 x 10) per carton, Rx Only, Distributed by: American Health Packaging, Columbus, Ohio 43217. Carton NDC#: 68084-447-01; Individual Dose NDC: 68084-447-11

Where it was distributed

Nationwide in the USA

Nationwide

Questions about this recall

Why was it recalled?

Failed Impurities/Degradation Specifications: Out of Specification results in the repackaged product for impurities at the 12-month time point.

Which lots are affected?

Lot#: 1007002, Exp 12/31/2023

Where was it sold?

Nationwide in the USA

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 III mean?

Class III recalls are for products unlikely to cause any adverse health consequence, usually labelling or quality issues.

Read the official FDA notice · Source record retrieved 26 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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