NDC 70839-112 Tekturna Hct

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:
70839-112
Proprietary Name:
Tekturna Hct
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Noden Pharma Usa, Inc.
Labeler Code:
70839
Start Marketing Date: [9]
08-01-2008
Listing Expiration Date: [11]
12-31-2023
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Characteristics

Color(s):
WHITE (C48325)
Shape:
OVAL (C48345)
Size(s):
15 MM
Imprint(s):
NVR;LCI
Score:
1

Product Details

What is NDC 70839-112?

The NDC code 70839-112 is assigned by the FDA to the product Tekturna Hct which is product labeled by Noden Pharma Usa, Inc.. The product's dosage form is . 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 Tekturna Hct?

This product is used to treat high blood pressure (hypertension). Lowering high blood pressure helps prevent strokes, heart attacks, and kidney problems. This product contains 2 medications: aliskiren and hydrochlorothiazide. Aliskiren works by relaxing blood vessels so blood can flow more easily. It belongs to a class of drugs known as direct renin inhibitors. Hydrochlorothiazide causes your body to get rid of extra salt and water by making more urine. It is called a "water pill" or diuretic.

Which are Tekturna Hct UNII Codes?

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

Which are Tekturna Hct 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 Tekturna Hct?

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: 1011710 - aliskiren 150 MG / hydroCHLOROthiazide 12.5 MG Oral Tablet
  • RxCUI: 1011710 - aliskiren 150 MG / hydrochlorothiazide 12.5 MG Oral Tablet
  • RxCUI: 1011710 - aliskiren 150 MG / HCTZ 12.5 MG Oral Tablet
  • RxCUI: 1011712 - Tekturna HCT 150 MG / 12.5 MG Oral Tablet
  • RxCUI: 1011712 - aliskiren 150 MG / hydrochlorothiazide 12.5 MG Oral Tablet [Tekturna HCT]

* 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".