NDC 54868-4142 Temodar
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Characteristics
WHITE (C48325)
YELLOW (C48330)
17 MM
TEMODAR;20;MG
Product Packages
NDC Code 54868-4142-0
Package Description: 5 CAPSULE in 1 BOTTLE
NDC Code 54868-4142-2
Package Description: 10 CAPSULE in 1 BOTTLE
NDC Code 54868-4142-3
Package Description: 60 CAPSULE in 1 BOTTLE
NDC Code 54868-4142-4
Package Description: 40 CAPSULE in 1 BOTTLE
NDC Code 54868-4142-5
Package Description: 30 CAPSULE in 1 BOTTLE
NDC Code 54868-4142-6
Package Description: 20 CAPSULE in 1 BOTTLE
Product Details
What is NDC 54868-4142?
What are the uses for Temodar?
Which are Temodar UNII Codes?
The UNII codes for the active ingredients in this product are:
- TEMOZOLOMIDE (UNII: YF1K15M17Y)
- TEMOZOLOMIDE (UNII: YF1K15M17Y) (Active Moiety)
Which are Temodar 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:
- ANHYDROUS LACTOSE (UNII: 3SY5LH9PMK)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- SODIUM STARCH GLYCOLATE TYPE A POTATO (UNII: 5856J3G2A2)
- TARTARIC ACID (UNII: W4888I119H)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- SHELLAC (UNII: 46N107B71O)
- ALCOHOL (UNII: 3K9958V90M)
- ISOPROPYL ALCOHOL (UNII: ND2M416302)
- BUTYL ALCOHOL (UNII: 8PJ61P6TS3)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- WATER (UNII: 059QF0KO0R)
- AMMONIA (UNII: 5138Q19F1X)
- POTASSIUM HYDROXIDE (UNII: WZH3C48M4T)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
- GELATIN (UNII: 2G86QN327L)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
- SODIUM LAURYL SULFATE (UNII: 368GB5141J)
- FD&C BLUE NO. 2 (UNII: L06K8R7DQK)
What is the NDC to RxNorm Crosswalk for Temodar?
- RxCUI: 261288 - Temodar 5 MG Oral Capsule
- RxCUI: 261288 - temozolomide 5 MG Oral Capsule [Temodar]
- RxCUI: 261289 - Temodar 20 MG Oral Capsule
- RxCUI: 261289 - temozolomide 20 MG Oral Capsule [Temodar]
- RxCUI: 261290 - Temodar 100 MG Oral Capsule
* 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".