NDC 21695-225 Lunesta
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 21695 - Rebel Distributors Corp
- 21695-225 - Lunesta
Product Characteristics
Product Packages
NDC Code 21695-225-30
Package Description: 30 TABLET, COATED in 1 BOTTLE
Product Details
What is NDC 21695-225?
What are the uses for Lunesta?
Which are Lunesta UNII Codes?
The UNII codes for the active ingredients in this product are:
- ESZOPICLONE (UNII: UZX80K71OE)
- ESZOPICLONE (UNII: UZX80K71OE) (Active Moiety)
Which are Lunesta 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:
- ANHYDROUS DIBASIC CALCIUM PHOSPHATE (UNII: L11K75P92J)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)
- HYPROMELLOSE 2910 (6 MPA.S) (UNII: 0WZ8WG20P6)
- LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)
- POLYETHYLENE GLYCOL (UNII: 3WJQ0SDW1A)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- TRIACETIN (UNII: XHX3C3X673)
What is the NDC to RxNorm Crosswalk for Lunesta?
- RxCUI: 485442 - eszopiclone 2 MG Oral Tablet
- RxCUI: 485465 - eszopiclone 3 MG Oral Tablet
- RxCUI: 540409 - Lunesta 2 MG Oral Tablet
- RxCUI: 540409 - eszopiclone 2 MG Oral Tablet [Lunesta]
- RxCUI: 540411 - Lunesta 3 MG 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".