Cinacalcet Tablet
NDC Package 43598-367-05

View Billable Units, 11-Digit Conversion Format, and RxNorm mappings
Table of Contents
    1. Package Information
    2. Other Packages
    3. Frequently Asked Questions

Package Information

Cinacalcet tablets is cinacalcet treatment initiation is contraindicated if serum calcium is less than the lower limit of the normal range [see Warnings and Precautions (5.1)]. This formulation utilizes a tablet delivery system. Marketed by Dr. Reddys Laboratories Inc, this product is identified by NDC 43598-367 and is authorized under FDA application ANDA208368.

Identification & Billing

NDC Package Code
43598-367-05
Package Description
500 TABLET in 1 BOTTLE
Product Code
43598-367
11-Digit Billing Format
43598036705
RxNorm Crosswalk

Clinical Specifications

Proprietary Name
Cinacalcet
Non-Proprietary Name
Cinacalcet
Substance Name
Cinacalcet Hydrochloride
Dosage Form
Tablet - A solid dosage form containing medicinal substances with or without suitable diluents.
Administration Route
Oral - Administration to or by way of the mouth.
Active Ingredient(s)
CINACALCET HYDROCHLORIDE 30 mg/1
Pharmacologic Class
Usage Information
Cinacalcet treatment initiation is contraindicated if serum calcium is less than the lower limit of the normal range [see Warnings and Precautions (5.1)].

Regulatory & Marketing

Labeler Name
Dr. Reddys Laboratories Inc
Product Type
Human Prescription Drug
FDA Application #
ANDA208368
Marketing Category
ANDA - A product marketed under an approved Abbreviated New Drug Application.
Start Marketing Date
09-18-2020
End Marketing Date
11-30-2026
Exclude Flag
N
Sample Package
No

Hierarchy Structure

Code Lineage

The NDC Directory contains ONLY information on final marketed drugs submitted to FDA electronically by labelers. A labeler might be a manufacturer, re-packager or re-labeler. The product information included in the NDC directory does not indicate that FDA has verified the information provided by the product labeler. Assigned NDC numbers are not in any way an indication of FDA approval of the product.

* Please review the full disclaimer at the bottom of this page.

Other Available Packages

The following commercial packages are registered under the same Product NDC (43598-367). Click a package code to view its specific billing and regulatory data.

43598-367-30
30 TABLET in 1 BOTTLE

* Please review the full disclaimer at the bottom of this page.

Frequently Asked Questions

What is the distribution configuration for this product package?

The code 43598-367-05 identifies a specific commercial package of 500 tablet in 1 bottle of Cinacalcet, a human prescription drug labeled by Dr. Reddys Laboratories Inc. This tablet is formulated for oral use and contains cinacalcet hydrochloride as the active substance.

Is this product currently listed with the FDA?

Yes, this product is active and verified within the NDC Directory. It was introduced to the market by Dr. Reddys Laboratories Inc on September 18, 2020.

How is this Dr. Reddys Laboratories Inc product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 43598036705. The table below illustrates the segment conversion from the 10-digit labeler code to the 11-digit provider format.

11-Digit Code Conversion

Billing payers usually require a 5-4-2 segment configuration. Below is the conversion from the 10-digit package format to the 11-digit billing format:

10-Digit Format (5-3-2)
43598-367-05
11-Digit CMS (5-4-2)
43598-0367-05

Note: The zero is added to the Product segment to maintain the 5-4-2 structure.