NDC 65193-180 Ephed Plus Liquid

View Dosage, Usage, Ingredients, Routes, UNII

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
65193-180
Proprietary Name:
Ephed Plus Liquid
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Code:
65193
Start Marketing Date: [9]
11-10-2017
Listing Expiration Date: [11]
12-31-2022
Exclude Flag: [12]
I
Code Navigator:

Product Characteristics

Color(s):
PURPLE (C48327 - PURPLE)
Flavor(s):
GRAPE (C73391)

Code Structure Chart

Product Details

What is NDC 65193-180?

The NDC code 65193-180 is assigned by the FDA to the product Ephed Plus Liquid which is product labeled by Dickey Consumer Products Dba Dmd. The product's dosage form is . The product is distributed in a single package with assigned NDC code 65193-180-57 60 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 Ephed Plus Liquid?

Uses  for temporary relief of mild symptoms of intermittent asthma:  wheezingtightness of chest , shortness of breath , helps loosen phlegm (mucus) and thinbronchial secretions to rid bronchial passageways of bothersome mucus, and to makecoughs more productive

Which are Ephed Plus Liquid UNII Codes?

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

Which are Ephed Plus Liquid 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 Ephed Plus Liquid?

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: 1988809 - ePHEDrine HCl 25 MG / guaiFENesin 400 MG in 60 mL Oral Solution
  • RxCUI: 1988809 - ephedrine hydrochloride 0.417 MG/ML / guaifenesin 6.67 MG/ML Oral Solution
  • RxCUI: 1988809 - ephedrine HCl 25 MG / guaifenesin 400 MG per 60 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".