NDC 51772-311 Lazanda

View Dosage, Usage, Ingredients, Routes, UNII

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
51772-311
Proprietary Name:
Lazanda
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Archimedes Pharma Us Inc.
Labeler Code:
51772
Start Marketing Date: [9]
10-17-2011
Listing Expiration Date: [11]
12-31-2018
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

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?

The NDC code 51772-311 is assigned by the FDA to the product Lazanda which is product labeled by Archimedes Pharma Us Inc.. The product's dosage form is . The product is distributed in 2 packages with assigned NDC codes 51772-311-01 1 bottle, spray in 1 carton / 8 spray in 1 bottle, spray, 51772-311-04 4 bottle, spray in 1 carton / 8 spray in 1 bottle, spray. This page includes all the important details about this product, including active and inactive ingredients, pharmagologic classes, product uses and characteristics, UNII information and RxNorm crosswalk.

What are the uses for Lazanda?

See also Warning section. This medication is used to help relieve sudden (breakthrough) cancer pain in people who are regularly taking moderate to large amounts of opioid pain medication. Fentanyl belongs to a class of drugs known as opioid analgesics. It works in the brain to change how your body feels and responds to pain. This medication should not be used to relieve mild or short-term pain (such as due to headache/migraine, dental procedures, surgery).

Which are Lazanda UNII Codes?

The UNII codes for the active ingredients in this product are:

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:

What is the NDC to RxNorm Crosswalk for Lazanda?

RxNorm is a normalized naming system for generic and branded drugs that assigns unique concept identifier(s) known as RxCUIs to NDC products.The NDC to RxNorm Crosswalk for this produdct indicates multiple concept unique identifiers (RXCUIs) are associated with this product:
  • 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.

Product Footnotes

[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".