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NDC 76420-524 Physician Ez Use Joint Tunnel And Trigger Kit

Ammonia,Lidocaine Hydrochloride,Triamcinolone Acetonide,Povidone-iodine Kit - View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 76420-524?
  4. Physician Ez Use Joint Tunnel And Trigger Kit Uses
  5. Active Ingredients UNII Codes
  6. Inactive Ingredients UNII Codes
  7. NDC to RxNorm Crosswalk

Product Information

NDC Product Code:
76420-524
Proprietary Name:
Physician Ez Use Joint Tunnel And Trigger Kit
Non-Proprietary Name: [1]
Ammonia, Lidocaine Hydrochloride, Triamcinolone Acetonide, Povidone-iodine
NDC Directory Status:
Human Prescription Drug
Product Type: [3]
ACTIVE PRODUCT INCLUDED in the NDC Directory
Dosage Form:
Kit - A packaged collection of related material.
Labeler Name: [5]
Asclemed Usa, Inc.
Labeler Code:
76420
Product Label ID:
e25cfc22-29ba-473f-88c4-3c88e9f6863b
Marketing Category: [8]
UNAPPROVED DRUG OTHER - An unapproved drug product in a marketing category that is not reflected on a particular list.
Start Marketing Date: [9]
07-01-2013
Listing Expiration Date: [11]
12-31-2024
Exclude Flag: [12]
N
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Product Details

What is NDC 76420-524?

The NDC code 76420-524 is assigned by the FDA to the product Physician Ez Use Joint Tunnel And Trigger Kit which is a human prescription drug product labeled by Asclemed Usa, Inc.. The generic name of Physician Ez Use Joint Tunnel And Trigger Kit is ammonia, lidocaine hydrochloride, triamcinolone acetonide, povidone-iodine. The product's dosage form is kit. The product is distributed in a single package with assigned NDC code 76420-524-01 1 kit in 1 carton * 25 vial in 1 carton (70121-1049-5) / 1 ml in 1 vial * .33 ml in 1 ampule * 100 packet in 1 box (53329-941-30) / 1 ml in 1 packet * 10 ampule in 1 carton (55150-158-72) / 2 ml in 1 ampule. 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 Physician Ez Use Joint Tunnel And Trigger Kit?

Kenalog-40 Injection is contraindicated in patients who are hypersensitive to any components of this product (see WARNINGS: General).Intramuscular corticosteroid preparations are contraindicated for idiopathic thrombocytopenic purpura. Lidocaine is contraindicated in patients with a known history of hypersensitivity to local anesthetics of the amide type.

Which are Physician Ez Use Joint Tunnel And Trigger Kit UNII Codes?

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

Which are Physician Ez Use Joint Tunnel And Trigger Kit 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 Physician Ez Use Joint Tunnel And Trigger Kit?

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:

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Product Footnotes

[1] What is the Non-Proprietary Name? - The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.

[3] What kind of product is this? - Indicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.

[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.

[8] What is the Marketing Category? - Product types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.

[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".