NDC 16590-071 Diazepam
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Characteristics
YELLOW (C48330)
BLUE (C48333)
2683;V
26584;V
Product Packages
NDC Code 16590-071-04
Package Description: 4 TABLET in 1 BOTTLE
NDC Code 16590-071-10
Package Description: 10 TABLET in 1 BOTTLE
NDC Code 16590-071-15
Package Description: 15 TABLET in 1 BOTTLE
NDC Code 16590-071-20
Package Description: 20 TABLET in 1 BOTTLE
NDC Code 16590-071-28
Package Description: 28 TABLET in 1 BOTTLE
NDC Code 16590-071-30
Package Description: 30 TABLET in 1 BOTTLE
NDC Code 16590-071-45
Package Description: 45 TABLET in 1 BOTTLE
NDC Code 16590-071-56
Package Description: 56 TABLET in 1 BOTTLE
NDC Code 16590-071-60
Package Description: 60 TABLET in 1 BOTTLE
NDC Code 16590-071-62
Package Description: 84 TABLET in 1 BOTTLE
NDC Code 16590-071-72
Package Description: 120 TABLET in 1 BOTTLE
NDC Code 16590-071-75
Package Description: 75 TABLET in 1 BOTTLE
NDC Code 16590-071-90
Package Description: 90 TABLET in 1 BOTTLE
Product Details
What is NDC 16590-071?
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:
- CALCIUM STEARATE (UNII: 776XM7047L)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)
- LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X)
- CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)
- D&C YELLOW NO. 10 (UNII: 35SW5USQ3G)
- FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
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".