NDC 69865-250 Nucynta ER
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Characteristics
BLUE (C48333 - LIGHT BLUE)
BLUE (C48333 - BLUE GREEN)
OMJ;100
OMJ;150
Code Structure Chart
Product Details
What is NDC 69865-250?
What are the uses for Nucynta ER?
Which are Nucynta ER UNII Codes?
The UNII codes for the active ingredients in this product are:
- TAPENTADOL HYDROCHLORIDE (UNII: 71204KII53)
- TAPENTADOL (UNII: H8A007M585) (Active Moiety)
Which are Nucynta 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:
- POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A)
- HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO)
- .ALPHA.-TOCOPHEROL (UNII: H4N855PNZ1)
- POLYVINYL ALCOHOL, UNSPECIFIED (UNII: 532B59J990)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- TALC (UNII: 7SEV7J4R1U)
- SHELLAC (UNII: 46N107B71O)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- FERROSOFERRIC OXIDE (UNII: XM0M87F357)
- FD&C BLUE NO. 2 (UNII: L06K8R7DQK)
- ALUMINUM OXIDE (UNII: LMI26O6933)
- FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
What is the NDC to RxNorm Crosswalk for Nucynta ER?
- RxCUI: 1148797 - tapentadol 100 MG 12HR Extended Release Oral Tablet
- RxCUI: 1148797 - 12 HR tapentadol 100 MG Extended Release Oral Tablet
- RxCUI: 1148800 - tapentadol 150 MG 12HR Extended Release Oral Tablet
- RxCUI: 1148800 - 12 HR tapentadol 150 MG Extended Release Oral Tablet
- RxCUI: 1148803 - tapentadol 200 MG 12HR Extended Release 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".