NDC 33261-172 Zolpidem Tartrate
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Characteristics
Product Packages
NDC Code 33261-172-00
Package Description: 10 TABLET in 1 BOTTLE
NDC Code 33261-172-02
Package Description: 120 TABLET in 1 BOTTLE
NDC Code 33261-172-12
Package Description: 12 TABLET in 1 BOTTLE
NDC Code 33261-172-14
Package Description: 14 TABLET in 1 BOTTLE
NDC Code 33261-172-15
Package Description: 15 TABLET in 1 BOTTLE
NDC Code 33261-172-20
Package Description: 20 TABLET in 1 BOTTLE
NDC Code 33261-172-30
Package Description: 30 TABLET in 1 BOTTLE
NDC Code 33261-172-42
Package Description: 42 TABLET in 1 BOTTLE
NDC Code 33261-172-60
Package Description: 60 TABLET in 1 BOTTLE
NDC Code 33261-172-90
Package Description: 90 TABLET in 1 BOTTLE
Product Details
What is NDC 33261-172?
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)
What is the NDC to RxNorm Crosswalk for Zolpidem Tartrate?
- RxCUI: 854873 - zolpidem tartrate 10 MG Oral Tablet
- RxCUI: 854876 - zolpidem tartrate 5 MG 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".