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  5. NDC Package Code: 17856-3120-1 Calcitriol

NDC Package 17856-3120-1 Calcitriol

View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. Frequently Asked Questions

Package Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.

Find all the important details about this NDC Package code, including the 11-Digit NDC Billing number, billing units, wholesale price, RxNorm crosswalk, active ingredients, pharmacologic clasess, etc.

NDC Package Code:
17856-3120-1
Package Description:
120 SYRINGE in 1 BOX, UNIT-DOSE / .5 mL in 1 SYRINGE
Product Code:
17856-3120
Proprietary Name:
Calcitriol
Usage Information:
Calcitriol is a man-made active form of vitamin D. Most people get enough vitamin D from exposure to the sun and from fortified food products (e.g., dairy products, vitamins). Vitamin D helps control parathyroid hormone and the levels of certain minerals (e.g., calcium, phosphorus) that are needed for building and keeping strong bones. Before regular vitamin D can be used by the body, it needs to be changed to the active form by the liver and kidneys. Calcitriol is used in patients with kidney disease who can't make enough of the active form of Vitamin D. This medication is also used to prevent and treat certain types of calcium/phosphorus/parathyroid problems that can happen with long-term kidney dialysis or hypoparathyroidism. Calcitriol is usually used along with specific diet recommendations and sometimes other medications.
11-Digit NDC Billing Format:
17856312001
NDC to RxNorm Crosswalk:
  • RxCUI: 313932 - calcitriol 1 MCG in 1 mL Oral Solution
  • RxCUI: 313932 - calcitriol 0.001 MG/ML Oral Solution
  • RxCUI: 313932 - calcitriol 1 MCG per 1 ML Oral Solution
    • Labeler Name:
    Atlantic Biologicals Corp.
    Sample Package:
    No
    Start Marketing Date:
    05-09-2019
    Listing Expiration Date:
    12-31-2022
    Exclude Flag:
    I
    Code Structure:

    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 disclaimer below.

    Frequently Asked Questions

    What is NDC 17856-3120-1?

    The NDC Packaged Code 17856-3120-1 is assigned to a package of 120 syringe in 1 box, unit-dose / .5 ml in 1 syringe of Calcitriol, labeled by Atlantic Biologicals Corp.. The product's dosage form is and is administered via form.

    Is NDC 17856-3120 included in the NDC Directory?

    No, Calcitriol with product code 17856-3120 is excluded from the NDC Directory because it's listing has been INACTIVATED by FDA. The product was first marketed by Atlantic Biologicals Corp. on May 09, 2019 and its listing in the NDC Directory is set to expire on December 31, 2022 if the product is not updated or renewed by the manufacturer.

    What is the 11-digit format for NDC 17856-3120-1?

    The 11-digit format is 17856312001. The 11-digit billing format might be required by the Centers for Medicare & Medicaid Services (CMS) and other payers in billing claim forms.

    This package code is originally configured in a 5-4-1 segment 10-digit format and by adding a zero within the original NDC package code we can obtain the converted 11-digit format in a 5-4-2 segment configuration. The table below shows the 11-digit code conversion:

    10-Digit Format10-Digit Original Code11-Digit Format11-Digit Code
    5-4-117856-3120-15-4-217856-3120-01