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

Is NDC 0054-0176-13 recalled?

Buprenorphine · 30 TABLET in 1 BOTTLE (0054-0176-13)

Yes — this exact package was recalled

1 FDA recall names the code 0054-0176-13 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
Buprenorphine
Strength
BUPRENORPHINE HYDROCHLORIDE 2 mg/1
Form
Tablet · Sublingual
Labeler
Hikma Pharmaceuticals USA Inc.
Type
Human Prescription Drug · DEA CIII
Product code
0054-0176

Recalls naming this package

Class II · Moderate risk

Buprenorphine HCL Sl

Labeling: Label Mixup: BUPRENORPHINE HCL SL, Tablet, 2 mg may be potentially mislabeled as one of the following drugs: DOCUSATE SODIUM, Capsule, 250 mg, NDC 00904789159, Pedigree: AD37072_4, EXP: 5/13/2014; MAGNESIUM CHLORIDE DR, Tablet, 64 mg, NDC 00904791152, Pedigree: AD54510_1, EXP: 2/28/2014.

Terminated Labeling / mix-up Aidapak Services, LLC D-796-2014

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