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  4. NDC Product Code: 0677-1979 Nisoldipine

NDC 0677-1979 Nisoldipine

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 0677-1979?
  5. Nisoldipine 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:
0677-1979
Proprietary Name:
Nisoldipine
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
United Research Laboratories, Inc.
Labeler Code:
0677
Product Label ID:
2abc5435-b2ca-4e08-89bc-ab7526781819
Start Marketing Date: [9]
09-01-2009
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Characteristics

Color(s):
GRAY (C48324 - OYSTER)
YELLOW (C48330 - YELLOW CREAM)
Shape:
ROUND (C48348)
Size(s):
7 MM
Imprint(s):
SCI;500
SCI;501
Score:
1

Product Packages

NDC Code 0677-1979-01

Package Description: 1 BOTTLE in 1 CARTON / 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE

Product Details

What is NDC 0677-1979?

The NDC code 0677-1979 is assigned by the FDA to the product Nisoldipine which is product labeled by United Research Laboratories, Inc.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 0677-1979-01 1 bottle in 1 carton / 100 tablet, film coated, extended release 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 Nisoldipine?

Nisoldipine is used with or without other medications to treat high blood pressure (hypertension). Lowering high blood pressure helps prevent strokes, heart attacks, and kidney problems. Nisoldipine is called a calcium channel blocker. It works by relaxing blood vessels so blood can flow more easily.

Which are Nisoldipine UNII Codes?

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

Which are Nisoldipine 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 Nisoldipine?

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: 763519 - nisoldipine 17 MG 24HR Extended Release Oral Tablet
  • RxCUI: 763519 - 24 HR nisoldipine 17 MG Extended Release Oral Tablet
  • RxCUI: 763519 - nisoldipine 17 MG 24 HR Extended Release Oral Tablet
  • RxCUI: 763574 - nisoldipine 25.5 MG 24HR Extended Release Oral Tablet
  • RxCUI: 763574 - 24 HR nisoldipine 25.5 MG Extended Release 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".