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  4. NDC Product Code: 60575-616 Codar GF

NDC 60575-616 Codar GF

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 60575-616?
  5. Codar GF 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:
60575-616
Proprietary Name:
Codar GF
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Respa Pharmaceuticals, Inc.
Labeler Code:
60575
Product Label ID:
6eda2c06-fb11-4a58-98fb-4eafe1d1df5f
Start Marketing Date: [9]
06-21-2011
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Navigator:

Product Characteristics

Flavor(s):
COTTON CANDY (C73382)

Code Structure Chart

Product Details

What is NDC 60575-616?

The NDC code 60575-616 is assigned by the FDA to the product Codar GF which is product labeled by Respa Pharmaceuticals, Inc.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 60575-616-16 473 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 Codar GF?

Take this medication with a full glass of water after each dose to help loosen mucus in the lungs.Adults and children12 years of ageand over:2 teaspoonfuls (10 mL)every 4 hours, not toexceed 12 teaspoonfuls in 24 hoursChildren 6 to under12 years of age:1 teaspoonful (5 mL)every 4 hours, not toexceed 6 teaspoonfulsin 24 hours*Children under 6years of ageConsult a doctor*Giving a higher dose than recommended by a doctor could result in serious side effects for your child.

Which are Codar GF UNII Codes?

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

Which are Codar GF 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 Codar GF?

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: 1114026 - codeine phosphate 8 MG / guaiFENesin 200 MG in 5 mL Oral Solution
  • RxCUI: 1114026 - codeine phosphate 1.6 MG/ML / guaifenesin 40 MG/ML Oral Solution
  • RxCUI: 1114026 - codeine phosphate 8 MG / guaifenesin 200 MG per 5 ML Oral Solution
  • RxCUI: 1114030 - codeine phosphate 1.6 MG/ML / guaifenesin 40 MG/ML Oral Solution [Codar GF]
  • RxCUI: 1114030 - Codar GF (codeine phosphate 8 MG / guaifenesin 200 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".