NDC 16590-215 Cefuroxime Axetil
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 16590 - Stat Rx Usa Llc
- 16590-215 - Cefuroxime Axetil
Product Characteristics
Product Packages
NDC Code 16590-215-20
Package Description: 20 TABLET, FILM COATED in 1 BOTTLE
Product Details
What is NDC 16590-215?
What are the uses for Cefuroxime Axetil?
Which are Cefuroxime Axetil UNII Codes?
The UNII codes for the active ingredients in this product are:
- CEFUROXIME AXETIL (UNII: Z49QDT0J8Z)
- CEFUROXIME (UNII: O1R9FJ93ED) (Active Moiety)
Which are Cefuroxime Axetil 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:
- CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)
- DIBUTYL SEBACATE (UNII: 4W5IH7FLNY)
- HYDROGENATED CASTOR OIL (UNII: ZF94AP8MEY)
- HYPROMELLOSES (UNII: 3NXW29V3WO)
- POLYSORBATE 80 (UNII: 6OZP39ZG8H)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- SHELLAC (UNII: 46N107B71O)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- SMCC (UNII: B357P1G1IF)
- SODIUM LAURYL SULFATE (UNII: 368GB5141J)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
What is the NDC to RxNorm Crosswalk for Cefuroxime Axetil?
- RxCUI: 309098 - cefuroxime axetil 500 MG Oral Tablet
- RxCUI: 309098 - cefuroxime 500 MG Oral Tablet
- RxCUI: 309098 - cefuroxime (as cefuroxime axetil) 500 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".