NDC 21695-022 Celebrex
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 21695 - Rebel Distributors Corp.
- 21695-022 - Celebrex
Product Characteristics
Product Packages
NDC Code 21695-022-00
Package Description: 100 BOTTLE in 1 BOTTLE / 60 CAPSULE in 1 BOTTLE (21695-022-60)
NDC Code 21695-022-15
Package Description: 15 CAPSULE in 1 BOTTLE
NDC Code 21695-022-30
Package Description: 30 CAPSULE in 1 BOTTLE
NDC Code 21695-022-72
Package Description: 120 CAPSULE in 1 BOTTLE
Product Details
What is NDC 21695-022?
What are the uses for Celebrex?
Which are Celebrex UNII Codes?
The UNII codes for the active ingredients in this product are:
- CELECOXIB (UNII: JCX84Q7J1L)
- CELECOXIB (UNII: JCX84Q7J1L) (Active Moiety)
Which are Celebrex 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)
- GELATIN (UNII: 2G86QN327L)
- LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- POVIDONE (UNII: FZ989GH94E)
- SODIUM LAURYL SULFATE (UNII: 368GB5141J)
What is the NDC to RxNorm Crosswalk for Celebrex?
- RxCUI: 205322 - celecoxib 100 MG Oral Capsule
- RxCUI: 205323 - celecoxib 200 MG Oral Capsule
- RxCUI: 213468 - CeleBREX 100 MG Oral Capsule
- RxCUI: 213468 - celecoxib 100 MG Oral Capsule [Celebrex]
- RxCUI: 213468 - Celebrex 100 MG Oral Capsule
* 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".