NDC 49252-034 Paliperidone
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 49252 - Inventia Healthcare Limited
- 49252-034 - Paliperidone
Product Characteristics
WHITE (C48325 - WHITE)
BROWN (C48332 - BEIGE)
033
034
Product Packages
NDC Code 49252-034-10
Package Description: 30 TABLET, EXTENDED RELEASE in 1 BOTTLE
Product Details
What is NDC 49252-034?
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:
- POLYETHYLENE GLYCOL (UNII: 3WJQ0SDW1A)
- CARBOMER HOMOPOLYMER TYPE A (ALLYL PENTAERYTHRITOL CROSSLINKED) (UNII: F68VH75CJC)
- CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)
- BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
- HYPROMELLOSE PHTHALATE (31% PHTHALATE, 40 CST) (UNII: G4U024CQK6)
- ETHYLCELLULOSES (UNII: 7Z8S9VYZ4B)
- DIBUTYL SEBACATE (UNII: 4W5IH7FLNY)
- TALC (UNII: 7SEV7J4R1U)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
What is the NDC to RxNorm Crosswalk for Paliperidone?
- RxCUI: 672567 - paliperidone 3 MG 24HR Extended Release Oral Tablet
- RxCUI: 672567 - 24 HR paliperidone 3 MG Extended Release Oral Tablet
- RxCUI: 672567 - paliperidone 3 MG 24 HR Extended Release Oral Tablet
- RxCUI: 672569 - paliperidone 6 MG 24HR Extended Release Oral Tablet
- RxCUI: 672569 - 24 HR paliperidone 6 MG Extended Release Oral Tablet
* 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".