NDC 16590-947 Endodan
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 16590 - Stat Rx Usa Llc
- 16590-947 - Endodan
Product Characteristics
Product Packages
NDC Code 16590-947-30
Package Description: 30 TABLET in 1 BOTTLE
NDC Code 16590-947-60
Package Description: 60 TABLET in 1 BOTTLE
NDC Code 16590-947-90
Package Description: 90 TABLET in 1 BOTTLE
Product Details
What is NDC 16590-947?
What are the uses for Endodan?
Which are Endodan UNII Codes?
The UNII codes for the active ingredients in this product are:
- OXYCODONE HYDROCHLORIDE (UNII: C1ENJ2TE6C)
- OXYCODONE (UNII: CD35PMG570) (Active Moiety)
- ASPIRIN (UNII: R16CO5Y76E)
- ASPIRIN (UNII: R16CO5Y76E) (Active Moiety)
Which are Endodan 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:
- D&C YELLOW NO. 10 (UNII: 35SW5USQ3G)
- FD&C YELLOW NO. 6 (UNII: H77VEI93A8)
- CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)
- STARCH, CORN (UNII: O8232NY3SJ)
What is the NDC to RxNorm Crosswalk for Endodan?
- RxCUI: 848768 - oxyCODONE 4.8355 MG / aspirin 325 MG Oral Tablet
- RxCUI: 848768 - aspirin 325 MG / oxycodone hydrochloride 4.84 MG Oral Tablet
- RxCUI: 848768 - ASA 325 MG / oxycodone hydrochloride 4.8355 MG Oral Tablet
- RxCUI: 848768 - ASA 325 MG / oxycodone hydrochloride 4.84 MG Oral Tablet
- RxCUI: 848928 - ENDODAN 4.84 MG / 325 MG Oral Tablet, Reformulated May 2009
* 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".