NDC Package 0032-1206-07 Creon

Pancrelipase Capsule, Delayed Release Pellets Oral - View Billable Units, 11-Digit Format, RxNorm

Package Information

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:
0032-1206-07
Package Description:
250 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE
Product Code:
Proprietary Name:
Creon
Non-Proprietary Name:
Pancrelipase
Substance Name:
Pancrelipase Amylase; Pancrelipase Lipase; Pancrelipase Protease
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:
00032120607
Billing Unit:
EA - Billing unit of "each" is used when the product is dispensed in discreet units.
NDC to RxNorm Crosswalk:
250 EA
NDC to RxNorm Crosswalk:
  • RxCUI: 1113042 - lipase 3000 UNT / amylase 15,000 UNT / protease 9500 UNT Delayed Release Oral Capsule
  • RxCUI: 1113042 - amylase 15000 UNT / lipase 3000 UNT / protease 9500 UNT Delayed Release Oral Capsule
  • RxCUI: 1113042 - amylase 15,000 UNT / lipase 3000 UNT / protease 9500 UNT Delayed Release Oral Capsule
  • RxCUI: 1113042 - amylases 15,000 UNT / endopeptidases 9500 UNT / lipase 3000 UNT Delayed Release Oral Capsule
  • RxCUI: 1113046 - CREON 3000 UNT / 15,000 UNT / 9500 UNT Delayed Release Oral Capsule
  • Product Type:
    Human Prescription Drug
    Labeler Name:
    Abbvie Inc.
    Dosage Form:
    Capsule, Delayed Release Pellets - A solid dosage form in which the drug is enclosed within either a hard or soft soluble container or "shell" made from a suitable form of gelatin; the drug itself is in the form of granules to which enteric coating has been applied, thus delaying release of the drug until its passage into the intestines.
    Administration Route(s):
  • Oral - Administration to or by way of the mouth.
  • Sample Package:
    No
    FDA Application Number:
    BLA020725
    Marketing Category:
    BLA - A product marketed under an approved Biologic License Application.
    Start Marketing Date:
    04-30-2009
    Listing Expiration Date:
    12-31-2025
    Exclude Flag:
    N
    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.

    Other Product Packages

    The following packages are also available for this product:

    NDC Package CodePackage Description
    0032-1206-011 BOTTLE in 1 CARTON / 100 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE
    0032-1206-561 BOTTLE in 1 CARTON / 100 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 0032-1206-07?

    The NDC Packaged Code 0032-1206-07 is assigned to a package of 250 capsule, delayed release pellets in 1 bottle of Creon, a human prescription drug labeled by Abbvie Inc.. The product's dosage form is capsule, delayed release pellets and is administered via oral form.

    Is NDC 0032-1206 included in the NDC Directory?

    Yes, Creon with product code 0032-1206 is active and included in the NDC Directory. The product was first marketed by Abbvie Inc. on April 30, 2009 and its listing in the NDC Directory is set to expire on December 31, 2025 if the product is not updated or renewed by the manufacturer.

    What is the NDC billing unit for package 0032-1206-07?

    The contents of this package are billed per "each", products billed on a per each basis are usually products dispensed in discreet units. The calculated billable units for this package is 250.

    What is the 11-digit format for NDC 0032-1206-07?

    The 11-digit format is 00032120607. 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 4-4-2 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
    4-4-20032-1206-075-4-200032-1206-07