NDC 68151-5652 Delzicol
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 68151 - Carilion Materials Management
- 68151-5652 - Delzicol
Product Characteristics
Product Packages
NDC Code 68151-5652-2
Package Description: 1 CAPSULE, DELAYED RELEASE in 1 PACKAGE
Product Details
What is NDC 68151-5652?
What are the uses for Delzicol?
Which are Delzicol UNII Codes?
The UNII codes for the active ingredients in this product are:
- MESALAMINE (UNII: 4Q81I59GXC)
- MESALAMINE (UNII: 4Q81I59GXC) (Active Moiety)
Which are Delzicol 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:
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- DIBUTYL SEBACATE (UNII: 4W5IH7FLNY)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
- FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
- LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- METHACRYLIC ACID - METHYL METHACRYLATE COPOLYMER (1:2) (UNII: 5KY68S2577)
- POLYETHYLENE GLYCOLS (UNII: 3WJQ0SDW1A)
- POVIDONES (UNII: FZ989GH94E)
- SODIUM STARCH GLYCOLATE TYPE A POTATO (UNII: 5856J3G2A2)
- TALC (UNII: 7SEV7J4R1U)
- HYPROMELLOSES (UNII: 3NXW29V3WO)
What is the NDC to RxNorm Crosswalk for Delzicol?
- RxCUI: 1368954 - mesalamine 400 MG Delayed Release Oral Capsule
- RxCUI: 1368960 - DELZICOL 400 MG Delayed Release Oral Capsule
- RxCUI: 1368960 - mesalamine 400 MG Delayed Release Oral Capsule [Delzicol]
- RxCUI: 1368960 - Delzicol 400 MG Delayed Release Oral Capsule
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[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".