NDC 54868-5426 Ambien Cr
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 54868 - Physicians Total Care, Inc.
- 54868-5426 - Ambien Cr
Product Characteristics
BLUE (C48333)
Product Packages
NDC Code 54868-5426-0
Package Description: 10 TABLET, COATED in 1 BOTTLE, PLASTIC
NDC Code 54868-5426-1
Package Description: 30 TABLET, COATED in 1 BOTTLE, PLASTIC
NDC Code 54868-5426-3
Package Description: 60 TABLET, COATED in 1 BOTTLE, PLASTIC
NDC Code 54868-5426-4
Package Description: 90 TABLET, COATED in 1 BOTTLE, PLASTIC
Product Details
What is NDC 54868-5426?
What are the uses for Ambien Cr?
Which are Ambien Cr UNII Codes?
The UNII codes for the active ingredients in this product are:
- ZOLPIDEM TARTRATE (UNII: WY6W63843K)
- ZOLPIDEM (UNII: 7K383OQI23) (Active Moiety)
Which are Ambien Cr 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)
- HYPROMELLOSES (UNII: 3NXW29V3WO)
- LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)
- POLYETHYLENE GLYCOLS (UNII: 3WJQ0SDW1A)
- POTASSIUM BITARTRATE (UNII: NPT6P8P3UU)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- FD&C BLUE NO. 2 (UNII: L06K8R7DQK)
- FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
What is the NDC to RxNorm Crosswalk for Ambien Cr?
- RxCUI: 854880 - zolpidem tartrate 12.5 MG Extended Release Oral Tablet
- RxCUI: 854882 - AMBIEN CR 12.5 MG Extended Release Oral Tablet
- RxCUI: 854882 - zolpidem tartrate 12.5 MG Extended Release Oral Tablet [Ambien]
- RxCUI: 854882 - Ambien CR 12.5 MG Extended Release Oral Tablet
- RxCUI: 854894 - zolpidem tartrate 6.25 MG Extended Release Oral Tablet
* 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".