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

Is NDC 0555-0071-02 recalled?

Isoniazid · 100 TABLET in 1 BOTTLE (0555-0071-02)

Yes — this exact package was recalled

1 FDA recall names the code 0555-0071-02 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
Isoniazid
Strength
ISONIAZID 300 mg/1
Form
Tablet · Oral
Labeler
Teva Pharmaceuticals USA, Inc.
Type
Human Prescription Drug
Product code
0555-0071

Recalls naming this package

Class II ยท Moderate risk

Isoniazid

Labeling: Label Mixup: ISONIAZID, Tablet, 300 mg may have potentially been mislabeled as one of the following drugs: hydrOXYzine PAMOATE, Capsule, 100 mg, NDC 00555032402, Pedigree: W003690, EXP: 6/26/2014; CETIRIZINE HCL, Tablet, 5 mg, NDC 00378363501, Pedigree: AD32757_13, EXP: 5/13/2014; RANOLAZINE ER, Tablet, 500 mg, NDC 61958100301, Pedigree: AD32757_47, EXP: 5/13/2014; DULoxetine HCl DR,

Terminated Labeling / mix-up Aidapak Services, LLC D-949-2014

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