NDC 54868-6196 Hydrocodone Polistirex And Chlorpheniramine Polistirex
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 54868 - Physicians Total Care, Inc.
- 54868-6196 - Hydrocodone Polistirex And Chlorpheniramine Polistirex
Product Characteristics
PINEAPPLE (C73409)
Product Packages
NDC Code 54868-6196-0
Package Description: 1 BOTTLE in 1 CARTON / 473 mL in 1 BOTTLE
Product Details
What is NDC 54868-6196?
What are the uses for Hydrocodone Polistirex And Chlorpheniramine Polistirex?
Which are Hydrocodone Polistirex And Chlorpheniramine Polistirex 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 Polistirex 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:
- ASCORBIC ACID (UNII: PQ6CK8PD0R)
- D&C YELLOW NO. 10 (UNII: 35SW5USQ3G)
- HIGH FRUCTOSE CORN SYRUP (UNII: XY6UN3QB6S)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- POLYSORBATE 80 (UNII: 6OZP39ZG8H)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- WATER (UNII: 059QF0KO0R)
- SODIUM ASCORBATE (UNII: S033EH8359)
- SODIUM METABISULFITE (UNII: 4VON5FNS3C)
- SODIUM POLYSTYRENE SULFONATE (UNII: 1699G8679Z)
- SUCROSE (UNII: C151H8M554)
- TRIACETIN (UNII: XHX3C3X673)
- XANTHAN GUM (UNII: TTV12P4NEE)
What is the NDC to RxNorm Crosswalk for Hydrocodone Polistirex And Chlorpheniramine Polistirex?
- 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.
[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".