NDC 21695-292 Ultram Er
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Characteristics
Code Structure Chart
Product Details
What is NDC 21695-292?
What are the uses for Ultram Er?
Which are Ultram Er UNII Codes?
The UNII codes for the active ingredients in this product are:
- TRAMADOL HYDROCHLORIDE (UNII: 9N7R477WCK)
- TRAMADOL (UNII: 39J1LGJ30J) (Active Moiety)
Which are Ultram Er 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:
- ETHYLCELLULOSES (UNII: 7Z8S9VYZ4B)
- DIBUTYL SEBACATE (UNII: 4W5IH7FLNY)
- 1-VINYL-2-PYRROLIDONE (UNII: 76H9G81541)
- SODIUM STEARYL FUMARATE (UNII: 7CV7WJK4UI)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- POLYVINYL ALCOHOL (UNII: 532B59J990)
What is the NDC to RxNorm Crosswalk for Ultram Er?
- RxCUI: 833709 - traMADol HCl 100 MG 24HR Extended Release Oral Tablet
- RxCUI: 833709 - 24 HR tramadol hydrochloride 100 MG Extended Release Oral Tablet
- RxCUI: 833709 - tramadol hydrochloride 100 MG 24 HR Extended Release Oral Tablet
- RxCUI: 833711 - traMADol HCl 200 MG 24HR Extended Release Oral Tablet
- RxCUI: 833711 - 24 HR tramadol hydrochloride 200 MG Extended Release 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".