NDC 21695-072 Risperidone
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 21695 - Rebel Distributors Corp
- 21695-072 - Risperidone
Product Characteristics
ORANGE (C48331 - ORANGE)
YELLOW (C48330 - YELLOW)
YELLOW (C48330)
13 MM
6 MM
R2;1038
R3;1039
O;25;1035
Product Packages
NDC Code 21695-072-60
Package Description: 60 TABLET in 1 BLISTER PACK
Product Details
What is NDC 21695-072?
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)
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".