NDC 68151-5041 Paliperidone
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 68151 - Carilion Materials Management
- 68151-5041 - Paliperidone
Product Characteristics
Product Packages
NDC Code 68151-5041-8
Package Description: 1 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE
Product Details
What is NDC 68151-5041?
What are the uses for Paliperidone?
Which are Paliperidone UNII Codes?
The UNII codes for the active ingredients in this product are:
- PALIPERIDONE (UNII: 838F01T721)
- PALIPERIDONE (UNII: 838F01T721) (Active Moiety)
Which are Paliperidone 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:
- BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)
- CELLULOSE ACETATE (UNII: 3J2P07GVB6)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- FD&C RED NO. 40 (UNII: WZB9127XOA)
- ALUMINUM OXIDE (UNII: LMI26O6933)
- HYDROXYPROPYL CELLULOSE (TYPE H) (UNII: RFW2ET671P)
- HYPROMELLOSES (UNII: 3NXW29V3WO)
- FERROSOFERRIC OXIDE (UNII: XM0M87F357)
- POLYETHYLENE GLYCOLS (UNII: 3WJQ0SDW1A)
- POVIDONES (UNII: FZ989GH94E)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
- POLYVINYL ALCOHOL (UNII: 532B59J990)
- TALC (UNII: 7SEV7J4R1U)
What is the NDC to RxNorm Crosswalk for Paliperidone?
- RxCUI: 672569 - paliperidone 6 MG 24HR Extended Release Oral Tablet
- RxCUI: 672569 - 24 HR paliperidone 6 MG Extended Release Oral Tablet
- RxCUI: 672569 - paliperidone 6 MG 24 HR Extended Release Oral Tablet
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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".