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

Is NDC 55513-0073-30 recalled?

Sensipar · 30 TABLET, COATED in 1 BOTTLE, PLASTIC (55513-073-30)

Yes — this exact package was recalled

2 FDA recalls name the code 55513-0073-30 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.

1 of these recalls is still ongoing.

Active ingredient
cinacalcet hydrochloride
Strength
CINACALCET HYDROCHLORIDE 30 mg/1
Form
Tablet, Coated · Oral
Labeler
Amgen Inc
Type
Human Prescription Drug
Product code
55513-0073

Recalls naming this package

Class II · Moderate risk

CINACALCET HCL Tablet

Labeling:Label Mixup; CINACALCET HCL, Tablet, 30 mg may be potentially mislabeled as ACETAMINOPHEN, Chew Tablet, 80 mg, NDC 00536323307, Pedigree: W003113, EXP: 6/13/2014; FERROUS SULFATE, Tablet, 325 mg (65 mg Elemental Iron), NDC 00904759160, Pedigree: AD54553_1, EXP: 5/20/2014; OMEGA-3-ACID ETHYL ESTERS, Capsule, 1000 mg, NDC 00173078302, Pedigree: AD32757_40, EXP: 5/14/2014; COLCHICINE,

Terminated Labeling / mix-up Aidapak Services, LLC D-624-2014

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