NDC 50090-4479 Zolpidem Tartrate
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 50090 - A-s Medication Solutions
- 50090-4479 - Zolpidem Tartrate
Product Characteristics
WHITE (C48325 - WHITE LAYER)
Product Packages
NDC Code 50090-4479-0
Package Description: 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE
Product Details
What is NDC 50090-4479?
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:
- LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X)
- MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)
- FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
- HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO)
- SODIUM STARCH GLYCOLATE TYPE A POTATO (UNII: 5856J3G2A2)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- TARTARIC ACID (UNII: W4888I119H)
- SHELLAC (UNII: 46N107B71O)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- BUTYL ALCOHOL (UNII: 8PJ61P6TS3)
- FERROSOFERRIC OXIDE (UNII: XM0M87F357)
- AMMONIA (UNII: 5138Q19F1X)
- TALC (UNII: 7SEV7J4R1U)
- POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A)
- POLYSORBATE 80 (UNII: 6OZP39ZG8H)
What is the NDC to RxNorm Crosswalk for Zolpidem Tartrate?
- RxCUI: 854880 - zolpidem tartrate 12.5 MG Extended Release Oral Tablet
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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.
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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".