NDC 17856-1206 Creon

View Dosage, Usage, Ingredients, Routes, UNII

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
17856-1206
Proprietary Name:
Creon
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Atlantic Biologicals Corps
Labeler Code:
17856
Start Marketing Date: [9]
08-13-2010
Listing Expiration Date: [11]
12-31-2018
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Characteristics

Color(s):
ORANGE (C48331 - ORANGE)
BLUE (C48333 - BLUE)
Shape:
OVAL (C48345)
Size(s):
14 MM
Imprint(s):
CREON;1206
Score:
1

Product Packages

NDC Code 17856-1206-1

Package Description: 1 CAPSULE, DELAYED RELEASE PELLETS in 1 POUCH

Product Details

What is NDC 17856-1206?

The NDC code 17856-1206 is assigned by the FDA to the product Creon which is product labeled by Atlantic Biologicals Corps. The product's dosage form is . The product is distributed in a single package with assigned NDC code 17856-1206-1 1 capsule, delayed release pellets in 1 pouch . This page includes all the important details about this product, including active and inactive ingredients, pharmagologic classes, product uses and characteristics, UNII information and RxNorm crosswalk.

What are the uses for Creon?

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).

Which are Creon UNII Codes?

The UNII codes for the active ingredients in this product are:

Which are Creon Inactive Ingredients UNII Codes?

The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product. The UNII codes for the inactive ingredients in this product are:

What is the NDC to RxNorm Crosswalk for Creon?

RxNorm is a normalized naming system for generic and branded drugs that assigns unique concept identifier(s) known as RxCUIs to NDC products.The NDC to RxNorm Crosswalk for this produdct indicates multiple concept unique identifiers (RXCUIs) are associated with this product:
  • RxCUI: 855499 - lipase 6000 UNT / amylase 30,000 UNT / protease 19,000 UNT Delayed Release Oral Capsule
  • RxCUI: 855499 - amylase 30000 UNT / lipase 6000 UNT / protease 19000 UNT Delayed Release Oral Capsule
  • RxCUI: 855499 - amylase 30,000 UNT / lipase 6000 UNT / protease 19,000 UNT Delayed Release Oral Capsule
  • RxCUI: 855499 - amylases 30,000 UNT / endopeptidases 19,000 UNT / lipase 6000 UNT Delayed Release Oral Capsule
  • RxCUI: 863836 - CREON 6000 UNT / 30,000 UNT / 19,000 UNT Delayed Release Oral Capsule

* Please review the disclaimer below.

Product Footnotes

[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.

[9] What is the Start Marketing Date? - This is the date that the labeler indicates was the start of its marketing of the drug product.

[11] What is the Listing Expiration Date? - This is the date when the listing record will expire if not updated or certified by the product labeler.

[12] What is the NDC Exclude Flag? - This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA"s requests for correction to deficient or non-compliant submissions ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".