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  4. NDC Product Code: 52083-681 G-dologen

NDC 52083-681 G-dologen

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 52083-681?
  5. G-dologen 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:
52083-681
Proprietary Name:
G-dologen
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Kramer Novis
Labeler Code:
52083
Product Label ID:
1bd74da3-9c5b-46e9-b599-999cd6eac1d8
Start Marketing Date: [9]
08-27-2014
Listing Expiration Date: [11]
12-31-2022
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Characteristics

Color(s):
WHITE (C48325 - IVORY WHITE)
Shape:
CAPSULE (C48336)
Size(s):
19 MM
Imprint(s):
D
Score:
2

Product Packages

NDC Code 52083-681-90

Package Description: 90 TABLET in 1 BOTTLE

Product Details

What is NDC 52083-681?

The NDC code 52083-681 is assigned by the FDA to the product G-dologen 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 52083-681-90 90 tablet 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 G-dologen?

UsesTemporarily relieves:• minor aches and pains associated with headache, the common cold,muscular aches, backache and minor pain from arthritis• runny nose and reduces sneezing, itching of the nose or throat, and itchy,watery eyes due to hay fever or other upper respiratory allergies

Which are G-dologen UNII Codes?

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

Which are G-dologen 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 G-dologen?

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: 1190931 - acetaminophen 650 MG / dexbrompheniramine maleate 2 MG Oral Tablet
  • RxCUI: 1190931 - APAP 650 MG / Dexbrompheniramine maleate 2 MG Oral Tablet

* 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".