NDC 17856-0205 Midazolam Hydrochloride
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 17856 - Atlantic Biologicals Corps
- 17856-0205 - Midazolam Hydrochloride
Product Packages
NDC Code 17856-0205-1
Package Description: 5 mL in 1 CUP
NDC Code 17856-0205-2
Package Description: 2 mL in 1 CUP
Product Details
What is NDC 17856-0205?
What are the uses for Midazolam Hydrochloride?
Which are Midazolam Hydrochloride UNII Codes?
The UNII codes for the active ingredients in this product are:
- MIDAZOLAM HYDROCHLORIDE (UNII: W7TTW573JJ)
- MIDAZOLAM (UNII: R60L0SM5BC) (Active Moiety)
Which are Midazolam Hydrochloride 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:
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- CHERRY (UNII: BUC5I9595W)
- D&C RED NO. 33 (UNII: 9DBA0SBB0L)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- GLYCERIN (UNII: PDC6A3C0OX)
- SODIUM BENZOATE (UNII: OJ245FE5EU)
- SODIUM CITRATE (UNII: 1Q73Q2JULR)
- SACCHARIN SODIUM DIHYDRATE (UNII: SB8ZUX40TY)
- SORBITOL (UNII: 506T60A25R)
- WATER (UNII: 059QF0KO0R)
What is the NDC to RxNorm Crosswalk for Midazolam Hydrochloride?
- RxCUI: 422410 - midazolam 10 MG in 5 mL Oral Solution
- RxCUI: 422410 - midazolam 2 MG/ML Oral Solution
- RxCUI: 422410 - midazolam (as midazolam hydrochloride) 10 MG per 5 ML Syrup
- RxCUI: 422410 - midazolam (as midazolam hydrochloride) 2 MG/ML Syrup
- RxCUI: 422410 - midazolam 10 MG per 5 ML Oral Solution
* Please review the disclaimer below.
Patient Education
Midazolam
Midazolam is given to children before medical procedures or before anesthesia for surgery to cause drowsiness, relieve anxiety, and prevent any memory of the event. Midazolam is in a class of medications called benzodiazepines. It works by slowing activity in the brain to allow relaxation and sleep.
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* 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".