NDC 35356-687 Nabumetone
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Characteristics
Product Packages
NDC Code 35356-687-00
Package Description: 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC
NDC Code 35356-687-14
Package Description: 14 TABLET, FILM COATED in 1 BOTTLE, PLASTIC
NDC Code 35356-687-15
Package Description: 15 TABLET, FILM COATED in 1 BOTTLE, PLASTIC
NDC Code 35356-687-20
Package Description: 20 TABLET, FILM COATED in 1 BOTTLE, PLASTIC
NDC Code 35356-687-30
Package Description: 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC
NDC Code 35356-687-60
Package Description: 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC
NDC Code 35356-687-90
Package Description: 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC
Product Details
What is NDC 35356-687?
What are the uses for Nabumetone?
Which are Nabumetone UNII Codes?
The UNII codes for the active ingredients in this product are:
- NABUMETONE (UNII: LW0TIW155Z)
- NABUMETONE (UNII: LW0TIW155Z) (Active Moiety)
Which are Nabumetone 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:
- COLLOIDAL SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- STARCH, CORN (UNII: O8232NY3SJ)
- HYPROMELLOSES (UNII: 3NXW29V3WO)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- POVIDONE (UNII: FZ989GH94E)
- SODIUM LAURYL SULFATE (UNII: 368GB5141J)
- SODIUM STARCH GLYCOLATE TYPE A POTATO (UNII: 5856J3G2A2)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- TRIACETIN (UNII: XHX3C3X673)
- TALC (UNII: 7SEV7J4R1U)
What is the NDC to RxNorm Crosswalk for Nabumetone?
- RxCUI: 311892 - nabumetone 500 MG Oral Tablet
* 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".