NDC 17856-3188 Diazepam
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 17856 - Atlantic Biologicals Corps
- 17856-3188 - Diazepam
Product Packages
NDC Code 17856-3188-1
Package Description: 60 SYRINGE in 1 BOX, UNIT-DOSE / .8 mL in 1 SYRINGE
NDC Code 17856-3188-2
Package Description: 2 mL in 1 CUP
NDC Code 17856-3188-3
Package Description: 120 SYRINGE in 1 BOX, UNIT-DOSE / .8 mL in 1 SYRINGE
NDC Code 17856-3188-4
Package Description: 72 CUP, UNIT-DOSE in 1 BOX, UNIT-DOSE / 5 mL in 1 CUP, UNIT-DOSE
Product Details
What is NDC 17856-3188?
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 CITRIC ACID (UNII: XF417D3PSL)
- D&C YELLOW NO. 10 (UNII: 35SW5USQ3G)
- FD&C RED NO. 40 (UNII: WZB9127XOA)
- POLYETHYLENE GLYCOL 1000 (UNII: U076Q6Q621)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- SODIUM CITRATE, UNSPECIFIED FORM (UNII: 1Q73Q2JULR)
- SORBITOL (UNII: 506T60A25R)
- WATER (UNII: 059QF0KO0R)
What is the NDC to RxNorm Crosswalk for Diazepam?
- RxCUI: 309843 - diazePAM 5 MG in 5 mL Oral Solution
- RxCUI: 309843 - diazepam 1 MG/ML Oral Solution
- RxCUI: 309843 - diazepam 5 MG per 5 ML Oral Solution
* 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".