NDC 17856-1206 Creon
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 17856 - Atlantic Biologicals Corps
- 17856-1206 - Creon
Product Characteristics
BLUE (C48333 - BLUE)
Product Packages
NDC Code 17856-1206-1
Package Description: 1 CAPSULE, DELAYED RELEASE PELLETS in 1 POUCH
Product Details
What is NDC 17856-1206?
What are the uses for Creon?
Which are Creon UNII Codes?
The UNII codes for the active ingredients in this product are:
- PANCRELIPASE LIPASE (UNII: 8MYC33932O)
- PANCRELIPASE LIPASE (UNII: 8MYC33932O) (Active Moiety)
- PANCRELIPASE PROTEASE (UNII: 3560D81V50)
- PANCRELIPASE PROTEASE (UNII: 3560D81V50) (Active Moiety)
- PANCRELIPASE AMYLASE (UNII: YOJ58O116E)
- PANCRELIPASE AMYLASE (UNII: YOJ58O116E) (Active Moiety)
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:
- CETYL ALCOHOL (UNII: 936JST6JCN)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- POLYETHYLENE GLYCOLS (UNII: 3WJQ0SDW1A)
- TRIETHYL CITRATE (UNII: 8Z96QXD6UM)
- HYPROMELLOSES (UNII: 3NXW29V3WO)
What is the NDC to RxNorm Crosswalk for Creon?
- 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.
[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".