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  5. NDC Package Code: 17856-1212-1 Creon

NDC Package 17856-1212-1 Creon

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:
17856-1212-1
Package Description:
1 CAPSULE, DELAYED RELEASE PELLETS in 1 POUCH
Product Code:
17856-1212
Proprietary Name:
Creon
Usage Information:
This medication contains digestive enzymes to help break down and digest fats, starch, and proteins in food. It is used in conditions where the pancreas cannot make or does not release enough digestive enzymes into the small intestines to digest the food (conditions such as chronic pancreatitis, cystic fibrosis, cancer of the pancreas, post-pancreatectomy, post-gastrointestinal bypass surgery).
11-Digit NDC Billing Format:
17856121201
NDC to RxNorm Crosswalk:
  • RxCUI: 855503 - lipase 12,000 UNT / amylase 60,000 UNT / protease 38,000 UNT Delayed Release Oral Capsule
  • RxCUI: 855503 - amylase 60000 UNT / lipase 12000 UNT / protease 38000 UNT Delayed Release Oral Capsule
  • RxCUI: 855503 - amylase 60,000 UNT / lipase 12,000 UNT / protease 38,000 UNT Delayed Release Oral Capsule
  • RxCUI: 855503 - amylases 60,000 UNT / endopeptidases 38,000 UNT / lipase 12,000 UNT Delayed Release Oral Capsule
  • RxCUI: 863841 - CREON 12,000 UNT / 60,000 UNT / 38,000 UNT Delayed Release Oral Capsule
    • Labeler Name:
    Atlantic Biologicals Corps
    Sample Package:
    No
    Start Marketing Date:
    08-13-2010
    Listing Expiration Date:
    12-31-2018
    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 17856-1212-1?

    The NDC Packaged Code 17856-1212-1 is assigned to a package of 1 capsule, delayed release pellets in 1 pouch of Creon, labeled by Atlantic Biologicals Corps. The product's dosage form is and is administered via form.

    Is NDC 17856-1212 included in the NDC Directory?

    No, Creon with product code 17856-1212 is excluded from the NDC Directory because it's listing has been INACTIVATED by FDA. The product was first marketed by Atlantic Biologicals Corps on August 13, 2010 and its listing in the NDC Directory is set to expire on December 31, 2018 if the product is not updated or renewed by the manufacturer.

    What is the 11-digit format for NDC 17856-1212-1?

    The 11-digit format is 17856121201. 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
    5-4-117856-1212-15-4-217856-1212-01