NDC 67046-657 Risperidone
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Characteristics
RED (C48326 - RED-BROWN)
WHITE (C48325 - WHITE TO OFF-WHITE)
ORANGE (C48331 - ORANGE)
YELLOW (C48330 - YELLOW)
6 MM
8 MM
10 MM
Z;6
ZC;75
ZC;76
ZC;77
Code Structure Chart
Product Details
What is NDC 67046-657?
What are the uses for Risperidone?
Which are Risperidone UNII Codes?
The UNII codes for the active ingredients in this product are:
- RISPERIDONE (UNII: L6UH7ZF8HC)
- RISPERIDONE (UNII: L6UH7ZF8HC) (Active Moiety)
Which are Risperidone 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:
- STARCH, CORN (UNII: O8232NY3SJ)
- HYPROMELLOSE (UNII: 3NXW29V3WO)
- LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)
- POLYETHYLENE GLYCOL (UNII: 3WJQ0SDW1A)
- SODIUM LAURYL SULFATE (UNII: 368GB5141J)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
- FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- FD&C YELLOW NO. 6 (UNII: H77VEI93A8)
- D&C YELLOW NO. 10 (UNII: 35SW5USQ3G)
What is the NDC to RxNorm Crosswalk for Risperidone?
- RxCUI: 312828 - risperiDONE 0.25 MG Oral Tablet
- RxCUI: 312828 - risperidone 0.25 MG Oral Tablet
- RxCUI: 312829 - risperiDONE 0.5 MG Oral Tablet
- RxCUI: 312829 - risperidone 0.5 MG Oral Tablet
- RxCUI: 312830 - risperiDONE 1 MG 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".