NDC 73684-101 Relafen
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 73684 - Blucrest Pharmaceuticals Llc
- 73684-101 - Relafen
Product Characteristics
Product Packages
NDC Code 73684-101-30
Package Description: 30 TABLET in 1 BOTTLE, PLASTIC
Product Details
What is NDC 73684-101?
What are the uses for Relafen?
Which are Relafen UNII Codes?
The UNII codes for the active ingredients in this product are:
- NABUMETONE (UNII: LW0TIW155Z)
- NABUMETONE (UNII: LW0TIW155Z) (Active Moiety)
Which are Relafen 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:
- POVIDONE, UNSPECIFIED (UNII: FZ989GH94E)
- HYDROXYPROPYL CELLULOSE (90000 WAMW) (UNII: UKE75GEA7F)
What is the NDC to RxNorm Crosswalk for Relafen?
- RxCUI: 206958 - Relafen 500 MG Oral Tablet
- RxCUI: 206958 - nabumetone 500 MG Oral Tablet [Relafen]
- RxCUI: 206959 - Relafen 750 MG Oral Tablet
- RxCUI: 206959 - nabumetone 750 MG Oral Tablet [Relafen]
- RxCUI: 311892 - nabumetone 500 MG Oral Tablet
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Patient Education
Nabumetone
Nabumetone 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). Nabumetone 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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* Please review the disclaimer below.
[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".