CLASS II ONGOING Drug recall · Reported 4 Mar 2026 · FDA Enforcement Report

Amantadine HCl, Capsules, UPS, 100 mg dose recalled by AvKARE

AvKARE is recalling Amantadine HCl, Capsules, UPS, 100 mg dose, distributed nationwide in the US. The recall was initiated on 13 Feb 2026 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesLot # 49261, Exp: 04/30/27
NDC50268-069
Quantity recalledN/A

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-0341-2026
FDA event ID
98449
Recalling firm
AvKARE, Pulaski, TN
Manufacturer
AvPAK
Classification
Class II
Status
Ongoing
Recall initiated
13 Feb 2026
FDA classified
23 Feb 2026
Reported
4 Mar 2026
Type
Voluntary: Firm initiated
Customers notified by
Letter
Reason category
Potency & Assay

Timeline

13 Feb 2026Recall initiated by company
23 Feb 2026Classified by FDA+10 days
4 Mar 2026Published in enforcement report+9 days

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

Reason for recall

Failed Dissolution Specifications: This recall has been initiated due to an Out of Specification finding in dissolution.

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

Amantadine HCl, Capsules, UPS, 100 mg, 50 Capsules (5 x 10) unit dose, Rx Only, Manufactured for: AvKARE, Pulaski, TN 38478, www.avkare.com, NDC 50268-069-15.

Where it was distributed

Nationwide in the USA.

Nationwide

Questions about this recall

Why was it recalled?

Failed Dissolution Specifications: This recall has been initiated due to an Out of Specification finding in dissolution.

Which lots are affected?

Lot # 49261, Exp: 04/30/27

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 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 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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