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  4. NDC Product Code: 67857-705 Tenex

NDC 67857-705 Tenex

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 67857-705?
  5. Tenex 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:
67857-705
Proprietary Name:
Tenex
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Promius Pharma, Llc
Labeler Code:
67857
Product Label ID:
886e050c-dd22-4f35-ac3b-243f091125c3
Start Marketing Date: [9]
10-27-1986
Listing Expiration Date: [11]
12-31-2018
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Characteristics

Color(s):
PINK (C48328)
Shape:
DIAMOND (C48338)
Size(s):
10 MM
Imprint(s):
TENEX;1;RP
Score:
1

Product Packages

NDC Code 67857-705-01

Package Description: 100 TABLET in 1 BOTTLE, PLASTIC

NDC Code 67857-705-05

Package Description: 500 TABLET in 1 BOTTLE, PLASTIC

Product Details

What is NDC 67857-705?

The NDC code 67857-705 is assigned by the FDA to the product Tenex which is product labeled by Promius Pharma, Llc. The product's dosage form is . The product is distributed in 2 packages with assigned NDC codes 67857-705-01 100 tablet in 1 bottle, plastic , 67857-705-05 500 tablet in 1 bottle, plastic . 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 Tenex?

Tenex (guanfacine hydrochloride) is indicated in the management of hypertension. Tenex may be given alone or in combination with other antihypertensive agents, especially thiazide-type diuretics.

Which are Tenex UNII Codes?

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

Which are Tenex 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 Tenex?

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:

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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".