NDC 54868-0059 Diazepam
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Characteristics
YELLOW (C48330)
3926;TEVA
Product Packages
NDC Code 54868-0059-0
Package Description: 60 TABLET in 1 BOTTLE
NDC Code 54868-0059-1
Package Description: 20 TABLET in 1 BOTTLE
NDC Code 54868-0059-2
Package Description: 30 TABLET in 1 BOTTLE
NDC Code 54868-0059-3
Package Description: 90 TABLET in 1 BOTTLE
NDC Code 54868-0059-4
Package Description: 100 TABLET in 1 BOTTLE
NDC Code 54868-0059-6
Package Description: 10 TABLET in 1 BOTTLE
NDC Code 54868-0059-8
Package Description: 6 TABLET in 1 BOTTLE
NDC Code 54868-0059-9
Package Description: 15 TABLET in 1 BOTTLE
Product Details
What is NDC 54868-0059?
What are the uses for Diazepam?
Which are Diazepam UNII Codes?
The UNII codes for the active ingredients in this product are:
- DIAZEPAM (UNII: Q3JTX2Q7TU)
- DIAZEPAM (UNII: Q3JTX2Q7TU) (Active Moiety)
Which are Diazepam 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)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)
- STARCH, CORN (UNII: O8232NY3SJ)
- SODIUM STARCH GLYCOLATE TYPE A POTATO (UNII: 5856J3G2A2)
- D&C YELLOW NO. 10 (UNII: 35SW5USQ3G)
- FD&C YELLOW NO. 6 (UNII: H77VEI93A8)
What is the NDC to RxNorm Crosswalk for Diazepam?
- RxCUI: 197589 - diazePAM 10 MG Oral Tablet
- RxCUI: 197589 - diazepam 10 MG Oral Tablet
- RxCUI: 197590 - diazePAM 2 MG Oral Tablet
- RxCUI: 197590 - diazepam 2 MG Oral Tablet
- RxCUI: 197591 - diazePAM 5 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".