1. Home
  2. Labeler Index
  3. Preferred Pharmaceuticals Inc.
  4. NDC Product Code: 68788-9975 Lidopro Patch

NDC 68788-9975 Lidopro Patch

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 68788-9975?
  4. Lidopro Patch Uses
  5. Active Ingredients UNII Codes
  6. Inactive Ingredients UNII Codes
  7. NDC to RxNorm Crosswalk

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
68788-9975
Proprietary Name:
Lidopro Patch
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Preferred Pharmaceuticals Inc.
Labeler Code:
68788
Product Label ID:
142e5b26-ca69-4546-b43d-88fb0e0bb385
Start Marketing Date: [9]
05-07-2015
Listing Expiration Date: [11]
12-31-2018
Exclude Flag: [12]
I
Code Navigator:

Code Structure Chart

Product Details

What is NDC 68788-9975?

The NDC code 68788-9975 is assigned by the FDA to the product Lidopro Patch which is product labeled by Preferred Pharmaceuticals Inc.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 68788-9975-1 3 pouch in 1 box / 5 patch in 1 pouch. 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 Lidopro Patch?

Adults 18 years and older:• Apply patch to affected area 1 to 2 times daily or as directed.

Which are Lidopro Patch UNII Codes?

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

Which are Lidopro Patch 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 Lidopro Patch?

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: 1599164 - lidocaine 4 % / menthol 5 % / methyl salicylate 4 % Medicated Patch
  • RxCUI: 1599164 - lidocaine 0.04 MG/MG / menthol 0.05 MG/MG / methyl salicylate 0.04 MG/MG Medicated Patch
  • RxCUI: 1599302 - LidoPro Patch 4 % / 5 % / 4 % Medicated Patch
  • RxCUI: 1599302 - lidocaine 0.04 MG/MG / menthol 0.05 MG/MG / methyl salicylate 0.04 MG/MG Medicated Patch [LidoPro Patch]
  • RxCUI: 1599302 - LidoPro Patch (lidocaine 4 % / menthol 5 % / methyl salicylate 4 % ) Medicated Patch

* 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".