Independent register of U.S. FDA drug recalls · updated Oct 10, 2026
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National Drug Code

Is NDC 64720-0128-10 recalled?

Pyridostigmine Bromide Tablets USP

Yes — this exact package was recalled

2 FDA recalls name the code 64720-0128-10 directly. A recall still applies to particular lot numbers — compare the lot on your package with the FDA notice below, and talk to your pharmacist before stopping a prescribed medication.

This code is not in the current FDA NDC directory — usual for a product that has since been discontinued or repackaged. The details below come from the recall notices themselves.

Recalls naming this package

Class II · Moderate risk

Pyridostigmine Bromide Tablets USP

Failed Dissolution Specification: Corepharma Inc. is recalling Pyridostigmine Bromide Tablets USP 60 mg due to an out of specification dissolution test generated at the 30 month stability time point.

Terminated Dissolution failure Corepharma LLC NDC 64720-128-10 D-1079-2014
Class II · Moderate risk

Pyridostigmine Bromide Tablets 60 mg

Failed Stability Specifications: Pyridostigmine Bromide tablets, is being recalled due to an out of specification test result during stablity testing.

Terminated Stability / shelf life Core Pharma Llc NDC 64720-128-10 D-1062-2013

Where to find this code. The NDC is printed on the pharmacy label and on the manufacturer's carton, usually as three groups of digits after “NDC”. The last group is the package size — two bottles of the same medicine can differ only in that group, and a recall may cover one but not the other.

Other recalled products from this labeler