NDC 60575-414 Tricode GF

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:
60575-414
Proprietary Name:
Tricode GF
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Respa Pharmaceuticals, Inc.
Labeler Code:
60575
Start Marketing Date: [9]
06-20-2011
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Characteristics

Flavor(s):
GRAPE (C73391)

Product Packages

NDC Code 60575-414-16

Package Description: 473 mL in 1 BOTTLE

Product Details

What is NDC 60575-414?

The NDC code 60575-414 is assigned by the FDA to the product Tricode 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 60575-414-16 473 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 Tricode GF?

Do not exceed recommended dosage.Adults and children12 years of ageand over:2 teaspoonfuls (10 mL)every 4 to 6 hours,not to exceed 8 teaspoonfuls in a 24 hour periodChildren 6 to under12 years of age:1 teaspoonful (5 mL)every 4 to 6 hours, not to exceed 4 teaspoonfulsin a 24 hour periodChildren under 6years of ageConsult a doctor.A special measuring device should be used to give an accurate dose of this product to children under 6 years of age.  Giving a higher dose than recommended by a doctor could result in serious side effects for your child.

Which are Tricode GF UNII Codes?

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

Which are Tricode 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 Tricode 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: 1114110 - codeine phosphate 8 MG / guaiFENesin 200 MG / pseudoephedrine HCl 30 MG in 5 mL Oral Solution
  • RxCUI: 1114110 - codeine phosphate 1.6 MG/ML / guaifenesin 40 MG/ML / pseudoephedrine hydrochloride 6 MG/ML Oral Solution
  • RxCUI: 1114110 - codeine phosphate 8 MG / guaifenesin 200 MG / pseudoephedrine hydrochloride 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".