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  4. NDC Product Code: 52083-625 Abatuss Dmx

NDC 52083-625 Abatuss Dmx

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 52083-625?
  5. Abatuss Dmx Uses
  6. Active Ingredients UNII Codes
  7. Inactive Ingredients UNII Codes
  8. NDC to RxNorm Crosswalk

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
52083-625
Proprietary Name:
Abatuss Dmx
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Kramer Novis
Labeler Code:
52083
Product Label ID:
6d54ef1e-6722-43f9-a0a7-14a786160b04
Start Marketing Date: [9]
05-25-2014
Listing Expiration Date: [11]
12-31-2023
Exclude Flag: [12]
I
Code Navigator:

Product Characteristics

Flavor(s):
GRAPE (C73391 - GRAPE FLAVOR)

Code Structure Chart

Product Details

What is NDC 52083-625?

The NDC code 52083-625 is assigned by the FDA to the product Abatuss Dmx which is product labeled by Kramer Novis. The product's dosage form is . The product is distributed in a single package with assigned NDC code 52083-625-16 1 bottle in 1 carton / 473 ml in 1 bottle. This page includes all the important details about this product, including active and inactive ingredients, pharmagologic classes, product uses and characteristics, UNII information and RxNorm crosswalk.

What are the uses for Abatuss Dmx?

Do not take more than 4 doses in any 24-hour periodEVERY 6 HOURSAdults and children 12 years of age and older:10 mL (2 tsp)Children 6 to under 12 years of age:5 mL (1 tsp)Children 2 to under 6 years of age:consult a physician

Which are Abatuss Dmx UNII Codes?

The UNII codes for the active ingredients in this product are:

  • DEXCHLORPHENIRAMINE MALEATE (UNII: B10YD955QW)
  • DEXCHLORPHENIRAMINE (UNII: 3Q9Q0B929N) (Active Moiety)
  • DEXTROMETHORPHAN HYDROBROMIDE (UNII: 9D2RTI9KYH)
  • DEXTROMETHORPHAN (UNII: 7355X3ROTS) (Active Moiety)
  • PSEUDOEPHEDRINE HYDROCHLORIDE (UNII: 6V9V2RYJ8N)
  • PSEUDOEPHEDRINE (UNII: 7CUC9DDI9F) (Active Moiety)

Which are Abatuss Dmx 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:

What is the NDC to RxNorm Crosswalk for Abatuss Dmx?

RxNorm is a normalized naming system for generic and branded drugs that assigns unique concept identifier(s) known as RxCUIs to NDC products.The NDC to RxNorm Crosswalk for this produdct indicates multiple concept unique identifiers (RXCUIs) are associated with this product:
  • RxCUI: 1298433 - dexchlorpheniramine maleate 1 MG / dextromethorphan HBr 15 MG / pseudoephedrine HCl 30 MG in 5 mL Oral Solution
  • RxCUI: 1298433 - dexchlorpheniramine maleate 0.2 MG/ML / dextromethorphan hydrobromide 3 MG/ML / pseudoephedrine hydrochloride 6 MG/ML Oral Solution
  • RxCUI: 1298433 - dexchlorpheniramine maleate 1 MG / dextromethorphan HBr 15 MG / pseudoephedrine HCl 30 MG per 5 ML Oral Solution

* Please review the disclaimer below.

Product Footnotes

[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".