NDC 50090-0522 Triazolam
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 50090 - A-s Medication Solutions
- 50090-0522 - Triazolam
Product Characteristics
Product Packages
NDC Code 50090-0522-0
Package Description: 30 TABLET in 1 BOTTLE
NDC Code 50090-0522-1
Package Description: 100 TABLET in 1 BOTTLE
NDC Code 50090-0522-3
Package Description: 6 TABLET in 1 BOTTLE
Product Details
What is NDC 50090-0522?
What are the uses for Triazolam?
Which are Triazolam UNII Codes?
The UNII codes for the active ingredients in this product are:
- TRIAZOLAM (UNII: 1HM943223R)
- TRIAZOLAM (UNII: 1HM943223R) (Active Moiety)
Which are Triazolam 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:
- POWDERED CELLULOSE (UNII: SMD1X3XO9M)
- STARCH, CORN (UNII: O8232NY3SJ)
- DOCUSATE SODIUM (UNII: F05Q2T2JA0)
- FD&C BLUE NO. 2 (UNII: L06K8R7DQK)
- LACTOSE, UNSPECIFIED FORM (UNII: J2B2A4N98G)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- SODIUM BENZOATE (UNII: OJ245FE5EU)
What is the NDC to RxNorm Crosswalk for Triazolam?
- RxCUI: 198318 - triazolam 0.25 MG Oral Tablet
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Patient Education
Triazolam
Triazolam is used on a short-term basis to treat insomnia (difficulty falling asleep or staying asleep). Triazolam is in a class of medications called benzodiazepines. It works by slowing activity in the brain to allow sleep.
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[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".