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  4. NDC Product Code: 52959-379 Diflunisal

NDC 52959-379 Diflunisal

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 52959-379?
  5. Diflunisal Uses
  6. Active Ingredients UNII Codes
  7. Inactive Ingredients UNII Codes
  8. NDC to RxNorm Crosswalk
  9. Patient Education

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
52959-379
Proprietary Name:
Diflunisal
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
H. J. Harkins Company Inc.
Labeler Code:
52959
Product Label ID:
60e0ecab-9cff-3b1b-e053-2a91aa0af663
Start Marketing Date: [9]
12-22-2017
Listing Expiration Date: [11]
12-31-2019
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Characteristics

Color(s):
BLUE (C48333)
Shape:
OVAL (C48345)
Size(s):
19 MM
Imprint(s):
755;93

Product Packages

NDC Code 52959-379-14

Package Description: 14 TABLET, FILM COATED in 1 CONTAINER

NDC Code 52959-379-15

Package Description: 15 TABLET, FILM COATED in 1 CONTAINER

NDC Code 52959-379-20

Package Description: 20 TABLET, FILM COATED in 1 CONTAINER

NDC Code 52959-379-21

Package Description: 21 TABLET, FILM COATED in 1 CONTAINER

NDC Code 52959-379-30

Package Description: 30 TABLET, FILM COATED in 1 CONTAINER

NDC Code 52959-379-60

Package Description: 60 TABLET, FILM COATED in 1 CONTAINER

NDC Code 52959-379-90

Package Description: 90 TABLET, FILM COATED in 1 CONTAINER

Product Details

What is NDC 52959-379?

The NDC code 52959-379 is assigned by the FDA to the product Diflunisal which is product labeled by H. J. Harkins Company Inc.. The product's dosage form is . The product is distributed in 7 packages with assigned NDC codes 52959-379-14 14 tablet, film coated in 1 container , 52959-379-15 15 tablet, film coated in 1 container , 52959-379-20 20 tablet, film coated in 1 container , 52959-379-21 21 tablet, film coated in 1 container , 52959-379-30 30 tablet, film coated in 1 container , 52959-379-60 60 tablet, film coated in 1 container , 52959-379-90 90 tablet, film coated in 1 container . 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 Diflunisal?

Diflunisal is used to relieve mild to moderate pain from various conditions. It also reduces pain, swelling, and joint stiffness caused by arthritis. Reducing these symptoms helps you do more of your normal daily activities. This medication is known as a nonsteroidal anti-inflammatory drug (NSAID).

Which are Diflunisal UNII Codes?

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

Which are Diflunisal 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 Diflunisal?

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 code indicates a single concept unique identifier (RXCUI) is associated with this product:

* Please review the disclaimer below.

Patient Education

Diflunisal


Diflunisal is used to relieve pain, tenderness, swelling and stiffness caused by osteoarthritis (arthritis caused by a breakdown of the lining of the joints) and rheumatoid arthritis (arthritis caused by swelling of the lining of the joints). Diflunisal is also used to relieve mild to moderate pain from other causes. Diflunisal is in a class of medications called NSAIDs. It works by stopping the body's production of a substance that causes pain, fever, and inflammation.
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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".