NDC 16590-987 Tolmetin Sodium
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 16590 - Stat Rx Usa Llc
- 16590-987 - Tolmetin Sodium
Product Characteristics
Product Packages
NDC Code 16590-987-30
Package Description: 30 TABLET, FILM COATED in 1 BOTTLE
NDC Code 16590-987-60
Package Description: 60 TABLET, FILM COATED in 1 BOTTLE
NDC Code 16590-987-90
Package Description: 90 TABLET, FILM COATED in 1 BOTTLE
Product Details
What is NDC 16590-987?
What are the uses for Tolmetin Sodium?
Which are Tolmetin Sodium UNII Codes?
The UNII codes for the active ingredients in this product are:
- TOLMETIN SODIUM (UNII: 02N1TZF99F)
- TOLMETIN (UNII: D8K2JPN18B) (Active Moiety)
Which are Tolmetin Sodium 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:
- FERROSOFERRIC OXIDE (UNII: XM0M87F357)
- CROSPOVIDONE (UNII: 68401960MK)
- HYPROMELLOSES (UNII: 3NXW29V3WO)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)
- POLYDEXTROSE (UNII: VH2XOU12IE)
- POLYETHYLENE GLYCOL (UNII: 3WJQ0SDW1A)
- POVIDONE (UNII: FZ989GH94E)
- STARCH, CORN (UNII: O8232NY3SJ)
- SODIUM LAURYL SULFATE (UNII: 368GB5141J)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- TRIACETIN (UNII: XHX3C3X673)
- FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
What is the NDC to RxNorm Crosswalk for Tolmetin Sodium?
- RxCUI: 198297 - tolmetin sodium 600 MG Oral Tablet
- RxCUI: 198297 - tolmetin 600 MG Oral Tablet
- RxCUI: 198297 - tolmetin 600 MG (as tolmetin sodium 738 MG) Oral Tablet
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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".