NDC 54868-6150 Apriso
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Characteristics
BLACK (C48323 - BLACK)
Code Structure Chart
Product Details
What is NDC 54868-6150?
What are the uses for Apriso?
Which are Apriso UNII Codes?
The UNII codes for the active ingredients in this product are:
- MESALAMINE (UNII: 4Q81I59GXC)
- MESALAMINE (UNII: 4Q81I59GXC) (Active Moiety)
Which are Apriso 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)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)
- HYPROMELLOSES (UNII: 3NXW29V3WO)
- METHACRYLIC ACID - METHYL METHACRYLATE COPOLYMER (1:1) (UNII: 74G4R6TH13)
- TALC (UNII: 7SEV7J4R1U)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- TRIETHYL CITRATE (UNII: 8Z96QXD6UM)
- ASPARTAME (UNII: Z0H242BBR1)
- ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)
- POVIDONE (UNII: FZ989GH94E)
What is the NDC to RxNorm Crosswalk for Apriso?
- RxCUI: 825130 - mesalamine 0.375 GM 24HR Extended Release Oral Capsule
- RxCUI: 825130 - 24 HR mesalamine 375 MG Extended Release Oral Capsule
- RxCUI: 825130 - mesalamine 375 MG 24 HR Extended Release Oral Capsule
- RxCUI: 825130 - mesalazine 375 MG 24 HR Extended Release Oral Capsule
- RxCUI: 825134 - Apriso 0.375 GM 24HR Extended 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".