1. Home
  2. Labeler Index
  3. Preferred Pharmaceuticals, Inc
  4. NDC Product Code: 68788-0852 Q-tapp Dm Elixir

NDC 68788-0852 Q-tapp Dm Elixir

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 68788-0852?
  5. Q-tapp Dm Elixir 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:
68788-0852
Proprietary Name:
Q-tapp Dm Elixir
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Preferred Pharmaceuticals, Inc
Labeler Code:
68788
Product Label ID:
0654b093-2067-492f-a0bc-647dac430bde
Start Marketing Date: [9]
04-05-2001
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Characteristics

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

Product Packages

NDC Code 68788-0852-0

Package Description: 118 mL in 1 BOTTLE, PLASTIC

Product Details

What is NDC 68788-0852?

The NDC code 68788-0852 is assigned by the FDA to the product Q-tapp Dm Elixir which is product labeled by Preferred Pharmaceuticals, Inc. The product's dosage form is . The product is distributed in a single package with assigned NDC code 68788-0852-0 118 ml in 1 bottle, plastic . 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 Q-tapp Dm Elixir?

Uses temporarily relieves cough due to minor throat and bronchial irritation occurring with a cold, and nasal congestion due to the common cold, hay fever or other upper respiratory allergies, or associated with sinusitis temporarily relieves symptoms due to hay fever (allergic rhinitis): runny nose sneezing itchy, watery eyes itching of the nose or throat temporarily restores freer breathing through the nose

Which are Q-tapp Dm Elixir UNII Codes?

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

Which are Q-tapp Dm Elixir 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 Q-tapp Dm Elixir?

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: 1098497 - brompheniramine maleate 1 MG / dextromethorphan HBr 5 MG / pseudoephedrine HCl 15 MG in 5 mL Oral Solution
  • RxCUI: 1098497 - brompheniramine maleate 0.2 MG/ML / dextromethorphan hydrobromide 1 MG/ML / pseudoephedrine hydrochloride 3 MG/ML Oral Solution
  • RxCUI: 1098497 - brompheniramine maleate 1 MG / dextromethorphan hydrobromide 5 MG / pseudoephedrine hydrochloride 15 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".