NDC 61919-514 Eszopiclone
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 61919 - Direct Rx
- 61919-514 - Eszopiclone
Product Characteristics
Product Packages
NDC Code 61919-514-30
Package Description: 30 TABLET, FILM COATED in 1 BOTTLE
Product Details
What is NDC 61919-514?
What are the uses for Eszopiclone?
Which are Eszopiclone UNII Codes?
The UNII codes for the active ingredients in this product are:
- ESZOPICLONE (UNII: UZX80K71OE)
- ESZOPICLONE (UNII: UZX80K71OE) (Active Moiety)
Which are Eszopiclone 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:
- CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)
- HYPROMELLOSE 2910 (6 MPA.S) (UNII: 0WZ8WG20P6)
- TRIACETIN (UNII: XHX3C3X673)
- POLYETHYLENE GLYCOL 3350 (UNII: G2M7P15E5P)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)
- ANHYDROUS DIBASIC CALCIUM PHOSPHATE (UNII: L11K75P92J)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- FD&C BLUE NO. 2 (UNII: L06K8R7DQK)
What is the NDC to RxNorm Crosswalk for Eszopiclone?
- RxCUI: 485465 - eszopiclone 3 MG Oral Tablet
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Patient Education
Eszopiclone
Eszopiclone is used to treat insomnia (difficulty falling asleep or staying asleep). Eszopiclone is in a class of medications called 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".