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  4. NDC Product Code: 45737-606 Biophex TR

NDC 45737-606 Biophex TR

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 45737-606?
  5. Biophex TR 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:
45737-606
Proprietary Name:
Biophex TR
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Advanced Generic Corporation
Labeler Code:
45737
Product Label ID:
81a4cf27-585b-484b-b0d8-4e21b4016418
Start Marketing Date: [9]
04-01-2014
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Navigator:

Product Characteristics

Color(s):
WHITE (C48325)
Shape:
OVAL (C48345)
Size(s):
18 MM
Imprint(s):
BP;AGC
Score:
1

Code Structure Chart

Product Details

What is NDC 45737-606?

The NDC code 45737-606 is assigned by the FDA to the product Biophex TR which is product labeled by Advanced Generic Corporation. The product's dosage form is . The product is distributed in a single package with assigned NDC code 45737-606-10 100 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 Biophex TR?

UsesTemporarily relieves these symptoms associated with a cough, the common cold, hay fever, or other upper respiratory allergieshelps loosen phlegm (mucus)loosens nasal congestionsthin bronchial secretionsdrain bronchial tubesmake coughs more productiveclears stuffy noseclear nasal passagewaysshrinks swollen membranes

Which are Biophex TR UNII Codes?

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

Which are Biophex TR 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 Biophex TR?

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: 1946782 - guaiFENesin 388 MG / phenylephrine HCl 10 MG Oral Tablet
  • RxCUI: 1946782 - guaifenesin 388 MG / phenylephrine hydrochloride 10 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".