NDC 17856-0235 Hydrocodone Polistirex And Chlorpheniramine Polisitrex
View Dosage, Usage, Ingredients, Routes, UNII
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What is NDC 17856-0235?
What are the uses for Hydrocodone Polistirex And Chlorpheniramine Polisitrex?
Which are Hydrocodone Polistirex And Chlorpheniramine Polisitrex UNII Codes?
The UNII codes for the active ingredients in this product are:
- HYDROCODONE BITARTRATE (UNII: NO70W886KK)
- HYDROCODONE (UNII: 6YKS4Y3WQ7) (Active Moiety)
- CHLORPHENIRAMINE MALEATE (UNII: V1Q0O9OJ9Z)
- CHLORPHENIRAMINE (UNII: 3U6IO1965U) (Active Moiety)
Which are Hydrocodone Polistirex And Chlorpheniramine Polisitrex 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:
- SODIUM POLYSTYRENE SULFONATE (UNII: 1699G8679Z)
- WATER (UNII: 059QF0KO0R)
- VINYL ACETATE (UNII: L9MK238N77)
- TRIACETIN (UNII: XHX3C3X673)
- SODIUM METABISULFITE (UNII: 4VON5FNS3C)
- POLYSORBATE 80 (UNII: 6OZP39ZG8H)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- XANTHAN GUM (UNII: TTV12P4NEE)
- ASCORBIC ACID (UNII: PQ6CK8PD0R)
- SODIUM ASCORBATE (UNII: S033EH8359)
- HIGH FRUCTOSE CORN SYRUP (UNII: XY6UN3QB6S)
- SUCROSE (UNII: C151H8M554)
- D&C YELLOW NO. 10 (UNII: 35SW5USQ3G)
- MODIFIED CORN STARCH (1-OCTENYL SUCCINIC ANHYDRIDE) (UNII: 461P5CJN6T)
What is the NDC to RxNorm Crosswalk for Hydrocodone Polistirex And Chlorpheniramine Polisitrex?
- RxCUI: 1087459 - HYDROcodone polistirex 10 MG / chlorpheniramine polistirex 8 MG in 5 mL 12HR Extended Release Oral Suspension
- RxCUI: 1087459 - 12 HR chlorpheniramine polistirex 1.6 MG/ML / hydrocodone polistirex 2 MG/ML Extended Release Suspension
- RxCUI: 1087459 - hydrocodone polistirex 10 MG / chlorpheniramine polistirex 8 MG per 5 ML 12HR Extended Release Oral Suspension
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[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.
[6] What is the FDA Application Number? - This corresponds to the NDA, ANDA, or BLA number reported by the labeler for products which have the corresponding Marketing Category designated. If the designated Marketing Category is OTC Monograph Final or OTC Monograph Not Final, then the Application number will be the CFR citation corresponding to the appropriate Monograph (e.g. “part 341”). For unapproved drugs, this field will be null.
[8] What is the Marketing Category? - Product types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.
[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".