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

Is NDC 0591-5335-01 recalled?

Trihexyphenidyl Hydrochloride · 100 TABLET in 1 BOTTLE, PLASTIC (0591-5335-01)

Yes — this exact package was recalled

1 FDA recall names the code 0591-5335-01 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.

Active ingredient
Trihexyphenidyl Hydrochloride
Strength
TRIHEXYPHENIDYL HYDROCHLORIDE 2 mg/1
Form
Tablet
Labeler
Actavis Pharma, Inc.
Type
Drug for Further Processing
Product code
0591-5335

Recalls naming this package

Class II · Moderate risk

Trihexyphenidyl HCL

Labeling: Label Mixup:TRIHEXYPHENIDYL HCL, Tablet, 1 mg (1/2 of 2 mg) may have potentially been mislabeled as the following drug: PERPHENAZINE, Tablet, 16 mg, NDC 00781104901, Pedigree: AD73525_22, EXP: 5/30/2014.

Terminated Labeling / mix-up Aidapak Services, LLC D-974-2014

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