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  4. NDC Product Code: 33261-904 Losartan Potassium And Hydrochlorothiazide

NDC 33261-904 Losartan Potassium And Hydrochlorothiazide

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 33261-904?
  5. Losartan Potassium And Hydrochlorothiazide 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:
33261-904
Proprietary Name:
Losartan Potassium And Hydrochlorothiazide
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Aidarex Pharmaceuticals Llc
Labeler Code:
33261
Product Label ID:
c5de8851-986c-4f0c-9262-556bee0b48c0
Start Marketing Date: [9]
10-06-2010
Listing Expiration Date: [11]
12-31-2019
Exclude Flag: [12]
I
Code Navigator:

Product Characteristics

Color(s):
YELLOW (C48330)
Shape:
ROUND (C48348)
Size(s):
10 MM
Imprint(s):
54;557
Score:
1

Code Structure Chart

Product Details

What is NDC 33261-904?

The NDC code 33261-904 is assigned by the FDA to the product Losartan Potassium And Hydrochlorothiazide which is product labeled by Aidarex Pharmaceuticals Llc. The product's dosage form is . The product is distributed in 2 packages with assigned NDC codes 33261-904-30 30 tablet in 1 bottle, plastic , 33261-904-90 90 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 Losartan Potassium And Hydrochlorothiazide?

Losartan Potassium and Hydrochlorothiazide Tablets USP are contraindicated in patients who are hypersensitive to any component of this product.Because of the hydrochlorothiazide component, this product is contraindicated in patients with anuria or hypersensitivity to other sulfonamide­derived drugs.Do not co-administer aliskiren with Losartan Potassium and Hydrochlorothialzide Tablets USP in patients with diabetes.

Which are Losartan Potassium And Hydrochlorothiazide UNII Codes?

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

Which are Losartan Potassium And Hydrochlorothiazide 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 Losartan Potassium And Hydrochlorothiazide?

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: 979471 - losartan potassium 100 MG / hydroCHLOROthiazide 25 MG Oral Tablet
  • RxCUI: 979471 - hydrochlorothiazide 25 MG / losartan potassium 100 MG Oral Tablet
  • RxCUI: 979471 - HCTZ 25 MG / Losartan K+ 100 MG Oral Tablet
  • RxCUI: 979471 - HCTZ 25 MG / Losartan Pot 100 MG Oral Tablet
  • RxCUI: 979471 - HCTZ 25 MG / losartan potassium 100 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".