NDC 33261-019 Celebrex
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 33261 - Aidarex Pharmaceuticals Llc
- 33261-019 - Celebrex
Product Characteristics
Product Packages
NDC Code 33261-019-30
Package Description: 30 CAPSULE in 1 BOTTLE, PLASTIC
NDC Code 33261-019-34
Package Description: 10 BOTTLE, PLASTIC in 1 CARTON / 10 CAPSULE in 1 BOTTLE, PLASTIC (33261-019-10)
NDC Code 33261-019-60
Package Description: 60 CAPSULE in 1 BOTTLE, PLASTIC
Product Details
What is NDC 33261-019?
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)
- POVIDONES (UNII: FZ989GH94E)
- SODIUM LAURYL SULFATE (UNII: 368GB5141J)
What is the NDC to RxNorm Crosswalk for Celebrex?
- RxCUI: 205323 - celecoxib 200 MG Oral Capsule
- RxCUI: 213469 - CeleBREX 200 MG Oral Capsule
- RxCUI: 213469 - celecoxib 200 MG Oral Capsule [Celebrex]
- RxCUI: 213469 - Celebrex 200 MG Oral Capsule
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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".