NDC 43378-106 Zodryl Ac 80
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 43378 - Codadose, Inc.
- 43378-106 - Zodryl Ac 80
Product Characteristics
Product Packages
NDC Code 43378-106-08
Package Description: 236 mL in 1 BOTTLE, PLASTIC
Product Details
What is NDC 43378-106?
What are the uses for Zodryl Ac 80?
Which are Zodryl Ac 80 UNII Codes?
The UNII codes for the active ingredients in this product are:
- CHLORPHENIRAMINE MALEATE (UNII: V1Q0O9OJ9Z)
- CHLORPHENIRAMINE (UNII: 3U6IO1965U) (Active Moiety)
- CODEINE PHOSPHATE (UNII: GSL05Y1MN6)
- CODEINE (UNII: Q830PW7520) (Active Moiety)
Which are Zodryl Ac 80 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:
- ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)
- FD&C RED NO. 40 (UNII: WZB9127XOA)
- TANNIC ACID (UNII: 28F9E0DJY6)
- GLYCERIN (UNII: PDC6A3C0OX)
- MAGNESIUM ALUMINUM SILICATE (UNII: 6M3P64V0NC)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- WATER (UNII: 059QF0KO0R)
- SODIUM CITRATE (UNII: 1Q73Q2JULR)
- SUCRALOSE (UNII: 96K6UQ3ZD4)
- XANTHAN GUM (UNII: TTV12P4NEE)
What is the NDC to RxNorm Crosswalk for Zodryl Ac 80?
- RxCUI: 995062 - codeine phosphate 1 MG/mL / chlorpheniramine maleate 0.2 MG/mL Oral Suspension
- RxCUI: 995062 - chlorpheniramine maleate 0.2 MG/ML / codeine phosphate 1 MG/ML Oral Suspension
- RxCUI: 995062 - chlorpheniramine maleate 0.2 MG / codeine phosphate 1 MG per 1 ML Oral Suspension
- RxCUI: 995064 - Zodryl AC 80, 1 MG / 0.2 MG per 1 mL Oral Suspension
- RxCUI: 995064 - chlorpheniramine maleate 0.2 MG/ML / codeine phosphate 1 MG/ML Oral Suspension [Zodryl AC]
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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".