NDC 67046-990 Buprenorphine Hydrochloride
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Characteristics
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Product Details
What is NDC 67046-990?
What are the uses for Buprenorphine Hydrochloride?
Which are Buprenorphine Hydrochloride UNII Codes?
The UNII codes for the active ingredients in this product are:
- BUPRENORPHINE HYDROCHLORIDE (UNII: 56W8MW3EN1)
- BUPRENORPHINE (UNII: 40D3SCR4GZ) (Active Moiety)
Which are Buprenorphine Hydrochloride 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:
- STARCH, CORN (UNII: O8232NY3SJ)
- SODIUM STEARYL FUMARATE (UNII: 7CV7WJK4UI)
- LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X)
- MANNITOL (UNII: 3OWL53L36A)
- ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)
- TRISODIUM CITRATE DIHYDRATE (UNII: B22547B95K)
- POVIDONE K30 (UNII: U725QWY32X)
What is the NDC to RxNorm Crosswalk for Buprenorphine Hydrochloride?
- RxCUI: 351264 - buprenorphine HCl 2 MG Sublingual Tablet
- RxCUI: 351264 - buprenorphine 2 MG Sublingual Tablet
- RxCUI: 351264 - buprenorphine 2 MG (as buprenorphine HCl 2.16 MG) Sublingual Tablet
- RxCUI: 351265 - buprenorphine HCl 8 MG Sublingual Tablet
- RxCUI: 351265 - buprenorphine 8 MG Sublingual 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".