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

Is NDC 0555-0159-02 recalled?

Chlordiazepoxide Hydrochloride · 100 CAPSULE in 1 BOTTLE (0555-0159-02)

Yes — this exact package was recalled

1 FDA recall names the code 0555-0159-02 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.

Active ingredient
Chlordiazepoxide Hydrochloride
Strength
CHLORDIAZEPOXIDE HYDROCHLORIDE 25 mg/1
Form
Capsule · Oral
Labeler
Teva Pharmaceuticals USA, Inc.
Type
Human Prescription Drug · DEA CIV
Product code
0555-0159

Recalls naming this package

Class II · Moderate risk

chlordiazePOXIDE HCl

Labeling: Label Mixup: chlordiazePOXIDE HCl, Capsule, 25 mg may have potentially been mislabeled as one of the following drugs: FLECAINIDE ACETATE, Tablet, 50 mg, NDC 65162064110, Pedigree: AD46414_16, EXP: 5/16/2014; CALCIUM ACETATE, Capsule, 667 mg, NDC 00054008826, Pedigree: AD49463_1, EXP: 5/16/2014; LACTOBACILLUS GG, Capsule, 0 mg, NDC 49100036374, Pedigree: W003173, EXP: 6/13/2014.

Terminated Labeling / mix-up Aidapak Services, LLC D-950-2014

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

  • 0555-0972 Dextroamphetamine Saccharate, Amphetamine Aspartate, Dextroamphetamine Sulfate and Amphetamine Sulfate 4
  • 0555-9123 Jolessa 3
  • 0555-0324 Hydroxyzine Pamoate 2
  • 0555-0777 Dextroamphetamine Saccharate, Amphetamine Aspartate, Dextroamphetamine Sulfate and Amphetamine Sulfate 2
  • 0555-0808 See recall 2
  • 0555-0899 Estradiol 2