NDC 54868-5707 Suboxone
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Characteristics
14 MM
B;8
Code Structure Chart
Product Details
What is NDC 54868-5707?
What are the uses for Suboxone?
Which are Suboxone UNII Codes?
The UNII codes for the active ingredients in this product are:
- BUPRENORPHINE HYDROCHLORIDE (UNII: 56W8MW3EN1)
- BUPRENORPHINE (UNII: 40D3SCR4GZ) (Active Moiety)
- NALOXONE HYDROCHLORIDE (UNII: F850569PQR)
- NALOXONE (UNII: 36B82AMQ7N) (Active Moiety)
Which are Suboxone 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:
- LACTOSE (UNII: J2B2A4N98G)
- MANNITOL (UNII: 3OWL53L36A)
- STARCH, CORN (UNII: O8232NY3SJ)
- POVIDONE K30 (UNII: U725QWY32X)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- SODIUM CITRATE (UNII: 1Q73Q2JULR)
- FD&C YELLOW NO. 6 (UNII: H77VEI93A8)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
What is the NDC to RxNorm Crosswalk for Suboxone?
- RxCUI: 1010608 - Suboxone 2 MG / 0.5 MG Sublingual Tablet
- RxCUI: 1010608 - buprenorphine 2 MG / naloxone 0.5 MG Sublingual Tablet [Suboxone]
- RxCUI: 1010608 - Suboxone 2/0.5 (as buprenorphine HCl / naloxone HCl dihydrate) Sublingual Tablet
- RxCUI: 1010608 - Suboxone 2/0.5 Sublingual Tablet
- RxCUI: 1010609 - Suboxone 8 MG / 2 MG Sublingual 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".