NDC 51772-311 Lazanda
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 51772 - Archimedes Pharma Us Inc.
- 51772-311 - Lazanda
Product Packages
NDC Code 51772-311-01
Package Description: 1 BOTTLE, SPRAY in 1 CARTON / 8 SPRAY in 1 BOTTLE, SPRAY
NDC Code 51772-311-04
Package Description: 4 BOTTLE, SPRAY in 1 CARTON / 8 SPRAY in 1 BOTTLE, SPRAY
Product Details
What is NDC 51772-311?
What are the uses for Lazanda?
Which are Lazanda UNII Codes?
The UNII codes for the active ingredients in this product are:
- FENTANYL CITRATE (UNII: MUN5LYG46H)
- FENTANYL (UNII: UF599785JZ) (Active Moiety)
Which are Lazanda 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:
- WATER (UNII: 059QF0KO0R)
- MANNITOL (UNII: 3OWL53L36A)
- PECTIN (UNII: 89NA02M4RX)
- SUCROSE (UNII: C151H8M554)
- PHENYLETHYL ALCOHOL (UNII: ML9LGA7468)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
What is the NDC to RxNorm Crosswalk for Lazanda?
- RxCUI: 1115573 - fentaNYL 100 MCG/ACTUAT Metered Dose Nasal Spray
- RxCUI: 1115573 - fentanyl 0.1 MG/ACTUAT Metered Dose Nasal Spray
- RxCUI: 1115573 - fentanyl (as fentanyl citrate) 100 MCG/ACTUAT Metered Dose Nasal Spray
- RxCUI: 1115575 - Lazanda 100 MCG/ACTUAT Metered Dose Nasal Spray
- RxCUI: 1115575 - fentanyl 0.1 MG/ACTUAT Metered Dose Nasal Spray [Lazanda]
* 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".