NDC 50090-0998 Chantix
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 50090 - A-s Medication Solutions
- 50090-0998 - Chantix
Product Characteristics
BLUE (C48333 - LIGHT BLUE)
10 MM
PFIZER;CHX;1;0
Product Packages
NDC Code 50090-0998-0
Package Description: 1 KIT in 1 KIT * 11 TABLET, FILM COATED in 1 BLISTER PACK * 42 TABLET, FILM COATED in 1 BLISTER PACK
Product Details
What is NDC 50090-0998?
What are the uses for Chantix?
Which are Chantix UNII Codes?
The UNII codes for the active ingredients in this product are:
- VARENICLINE TARTRATE (UNII: 82269ASB48)
- VARENICLINE (UNII: W6HS99O8ZO) (Active Moiety)
Which are Chantix 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:
- MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)
- ANHYDROUS DIBASIC CALCIUM PHOSPHATE (UNII: L11K75P92J)
- CROSCARMELLOSE (UNII: 029TFK992N)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
What is the NDC to RxNorm Crosswalk for Chantix?
- RxCUI: 636671 - varenicline 0.5 MG Oral Tablet
- RxCUI: 636671 - varenicline 0.5 MG (as varenicline tartrate 0.85 MG) Oral Tablet
- RxCUI: 636676 - varenicline 1 MG Oral Tablet
- RxCUI: 636676 - varenicline 1 MG (as varenicline tartrate 1.71 MG) Oral Tablet
- RxCUI: 637188 - CHANTIX 0.5 MG Oral Tablet
* Please review the disclaimer below.
Patient Education
Varenicline
Varenicline is used along with education and counseling to help people stop smoking. Varenicline is in a class of medications called smoking cessation aids. It works by blocking the pleasant effects of nicotine (from smoking) on the brain.
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* 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".