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

Is NDC 14789-0300-02 recalled?

Benztropine Mesylate Injection

Yes — this exact package was recalled

2 FDA recalls name the code 14789-0300-02 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

Benztropine Mesylate Injection

Presence of particulate matter: characterized as thin colorless flakes that are visually and chemically consistent with glass delamination.

Terminated Particulate / foreign matter Nexus Pharmaceuticals Inc NDC 14789-300-02 D-925-2013
Class II · Moderate risk

Benztropine Mesylate Injection

Presence of particulate matter: characterized as thin colorless flakes that are visually and chemically consistent with glass delamination observed in reserve sample vials

Terminated Particulate / foreign matter Fresenius Kabi USA, LLC NDC 63323-970-02 D-685-2013

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