1. Home
  2. Labeler Index
  3. Blenheim Pharmacal, Inc.
  4. NDC Product Code: 10544-174 Bisoprolol Fumarate And Hydrochlorothiazide

NDC 10544-174 Bisoprolol Fumarate And Hydrochlorothiazide

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 10544-174?
  5. Bisoprolol Fumarate 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:
10544-174
Proprietary Name:
Bisoprolol Fumarate And Hydrochlorothiazide
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Blenheim Pharmacal, Inc.
Labeler Code:
10544
Product Label ID:
7e310381-d7dd-410f-9064-31bcea2dcc87
Start Marketing Date: [9]
11-15-2013
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Navigator:

Product Characteristics

Color(s):
YELLOW (C48330)
PINK (C48328)
WHITE (C48325)
Shape:
ROUND (C48348)
Size(s):
8 MM
Imprint(s):
UL;L
UL;LL
UL;LLL
Score:
1

Code Structure Chart

Product Details

What is NDC 10544-174?

The NDC code 10544-174 is assigned by the FDA to the product Bisoprolol Fumarate And Hydrochlorothiazide which is product labeled by Blenheim Pharmacal, Inc.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 10544-174-90 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 Bisoprolol Fumarate And Hydrochlorothiazide?

Bisoprolol fumarate and hydrochlorothiazide tablets are indicated in the management of hypertension.

Which are Bisoprolol Fumarate And Hydrochlorothiazide UNII Codes?

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

Which are Bisoprolol Fumarate 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 Bisoprolol Fumarate 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: 854908 - bisoprolol fumarate 10 MG / hydroCHLOROthiazide 6.25 MG Oral Tablet
  • RxCUI: 854908 - bisoprolol fumarate 10 MG / hydrochlorothiazide 6.25 MG Oral Tablet
  • RxCUI: 854908 - bisoprolol fumarate 10 MG / HCTZ 6.25 MG Oral Tablet
  • RxCUI: 854916 - bisoprolol fumarate 2.5 MG / hydroCHLOROthiazide 6.25 MG Oral Tablet
  • RxCUI: 854916 - bisoprolol fumarate 2.5 MG / hydrochlorothiazide 6.25 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".