NDC 53217-138 Buprenorphine And Naloxone
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 53217 - Aidarex Pharmaceuticals Llc
- 53217-138 - Buprenorphine And Naloxone
Product Characteristics
LIME (C73398 - LIME FLAVOR)
Product Packages
NDC Code 53217-138-30
Package Description: 30 TABLET in 1 BOTTLE
Product Details
What is NDC 53217-138?
What are the uses for Buprenorphine And Naloxone?
Which are Buprenorphine And Naloxone 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 Buprenorphine And Naloxone 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)
- MANNITOL (UNII: 3OWL53L36A)
- STARCH, CORN (UNII: O8232NY3SJ)
- POVIDONE K30 (UNII: U725QWY32X)
- WATER (UNII: 059QF0KO0R)
- ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)
- SODIUM CITRATE (UNII: 1Q73Q2JULR)
- SODIUM STEARYL FUMARATE (UNII: 7CV7WJK4UI)
- ACESULFAME POTASSIUM (UNII: 23OV73Q5G9)
What is the NDC to RxNorm Crosswalk for Buprenorphine And Naloxone?
- RxCUI: 351267 - buprenorphine HCl 8 MG / naloxone HCl 2 MG Sublingual Tablet
- RxCUI: 351267 - buprenorphine 8 MG / naloxone 2 MG Sublingual Tablet
- RxCUI: 351267 - buprenorphine 8 MG (as buprenorphine HCl) / naloxone 2 MG (as naloxone HCl) 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".