NDC 61919-955 Zolpidem Tartrate
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 61919 - Direct Rx
- 61919-955 - Zolpidem Tartrate
Product Characteristics
Product Packages
NDC Code 61919-955-30
Package Description: 30 TABLET, EXTENDED RELEASE in 1 BOTTLE
Product Details
What is NDC 61919-955?
What are the uses for Zolpidem Tartrate?
Which are Zolpidem Tartrate UNII Codes?
The UNII codes for the active ingredients in this product are:
- ZOLPIDEM TARTRATE (UNII: WY6W63843K)
- ZOLPIDEM (UNII: 7K383OQI23) (Active Moiety)
Which are Zolpidem Tartrate 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:
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- HYDROXYPROPYL CELLULOSE (TYPE H) (UNII: RFW2ET671P)
- HYPROMELLOSES (UNII: 3NXW29V3WO)
- LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- POLYETHYLENE GLYCOLS (UNII: 3WJQ0SDW1A)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
- TALC (UNII: 7SEV7J4R1U)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
What is the NDC to RxNorm Crosswalk for Zolpidem Tartrate?
- RxCUI: 854880 - zolpidem tartrate 12.5 MG Extended Release Oral Tablet
* Please review the disclaimer below.
Patient Education
Zolpidem
Zolpidem is used to treat insomnia (difficulty falling asleep or staying asleep). Zolpidem belongs to a class of medications called sedative-hypnotics. It works by slowing activity in the brain to allow sleep.
[Learn More]
* 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".