NDC 50090-3563 Temazepam
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 50090 - A-s Medication Solutions
- 50090-3563 - Temazepam
Product Characteristics
Product Packages
NDC Code 50090-3563-0
Package Description: 30 CAPSULE in 1 BOTTLE
Product Details
What is NDC 50090-3563?
What are the uses for Temazepam?
Which are Temazepam UNII Codes?
The UNII codes for the active ingredients in this product are:
- TEMAZEPAM (UNII: CHB1QD2QSS)
- TEMAZEPAM (UNII: CHB1QD2QSS) (Active Moiety)
Which are Temazepam 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:
- FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
- FD&C RED NO. 3 (UNII: PN2ZH5LOQY)
- GELATIN, UNSPECIFIED (UNII: 2G86QN327L)
- LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- BUTYL ALCOHOL (UNII: 8PJ61P6TS3)
- SHELLAC (UNII: 46N107B71O)
- ALUMINUM OXIDE (UNII: LMI26O6933)
- ISOPROPYL ALCOHOL (UNII: ND2M416302)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- ALCOHOL (UNII: 3K9958V90M)
- ETHYL ACETATE (UNII: 76845O8NMZ)
What is the NDC to RxNorm Crosswalk for Temazepam?
- RxCUI: 485489 - temazepam 22.5 MG Oral Capsule
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Patient Education
Temazepam
Temazepam is used on a short-term basis to treat insomnia (difficulty falling asleep or staying asleep). Temazepam 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".