NDC 71335-0950 Buprenorphine
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Characteristics
Code Structure Chart
Product Details
What is NDC 71335-0950?
What are the uses for Buprenorphine?
Which are Buprenorphine 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 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 MONOHYDRATE (UNII: EWQ57Q8I5X)
- POVIDONE K30 (UNII: U725QWY32X)
- ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)
- TRISODIUM CITRATE DIHYDRATE (UNII: B22547B95K)
- STARCH, CORN (UNII: O8232NY3SJ)
- MANNITOL (UNII: 3OWL53L36A)
- CROSPOVIDONE, UNSPECIFIED (UNII: 2S7830E561)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
What is the NDC to RxNorm Crosswalk for Buprenorphine?
- 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
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Patient Education
Buprenorphine Sublingual and Buccal (opioid dependence)
Buprenorphine and the combination of buprenorphine and naloxone are used to treat opioid dependence (addiction to opioid drugs, including heroin and narcotic painkillers). Buprenorphine is in a class of medications called opioid partial agonist-antagonists and naloxone is in a class of medications called opioid antagonists. Buprenorphine alone and the combination of buprenorphine and naloxone work to prevent withdrawal symptoms when someone stops taking opioid drugs by producing similar effects to these drugs.
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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".