NDC 52959-379 Diflunisal
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Characteristics
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?
What are the uses for Diflunisal?
Which are Diflunisal UNII Codes?
The UNII codes for the active ingredients in this product are:
- DIFLUNISAL (UNII: 7C546U4DEN)
- DIFLUNISAL (UNII: 7C546U4DEN) (Active Moiety)
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:
- INDIGOTINDISULFONATE SODIUM (UNII: D3741U8K7L)
- STARCH, CORN (UNII: O8232NY3SJ)
- MONOSTEARYL FUMARATE (UNII: X127TT7PK9)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- HYPROMELLOSE 2910 (15 MPA.S) (UNII: 36SFW2JZ0W)
- HYPROMELLOSE 2910 (6 MPA.S) (UNII: 0WZ8WG20P6)
- CROSCARMELLOSE (UNII: 029TFK992N)
- FD&C BLUE NO. 2 (UNII: L06K8R7DQK)
- CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
What is the NDC to RxNorm Crosswalk for Diflunisal?
- RxCUI: 197603 - diflunisal 500 MG Oral Tablet
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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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[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".