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  4. NDC Product Code: 51004-2010 Lidocaine Hydrochloride And Epinephrine Bitartrate

NDC 51004-2010 Lidocaine Hydrochloride And Epinephrine Bitartrate

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 51004-2010?
  4. Lidocaine Hydrochloride And Epinephrine Bitartrate 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:
51004-2010
Proprietary Name:
Lidocaine Hydrochloride And Epinephrine Bitartrate
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Novocol Pharmaceutical Of Canada, Inc.
Labeler Code:
51004
Product Label ID:
e38e35cc-f8d2-41ad-9477-748461aef348
Start Marketing Date: [9]
11-07-2011
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 51004-2010-5

Package Description: 50 CARTRIDGE in 1 CARTON / 1.7 mL in 1 CARTRIDGE

Product Details

What is NDC 51004-2010?

The NDC code 51004-2010 is assigned by the FDA to the product Lidocaine Hydrochloride And Epinephrine Bitartrate which is product labeled by Novocol Pharmaceutical Of Canada, Inc.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 51004-2010-5 50 cartridge in 1 carton / 1.7 ml in 1 cartridge. 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 Lidocaine Hydrochloride And Epinephrine Bitartrate?

Lidocaine and Epinephrine Injection, USP is indicated for the production of local anesthesia for dental procedures by nerve block or infiltration techniques.Only accepted procedures for these techniques as described in standard textbooks are recommended.

Which are Lidocaine Hydrochloride And Epinephrine Bitartrate UNII Codes?

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

Which are Lidocaine Hydrochloride And Epinephrine Bitartrate 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 Lidocaine Hydrochloride And Epinephrine Bitartrate?

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: 1293648 - lidocaine HCl 2 % / EPINEPHrine 1:100,000 in 1.7 mL Dental Cartridge
  • RxCUI: 1293648 - 1.7 ML epinephrine 0.01 MG/ML / lidocaine hydrochloride 20 MG/ML Cartridge
  • RxCUI: 1293648 - lidocaine HCl 2 % / epinephrine 1:100,000 1.7 ML Dental Cartridge
  • RxCUI: 1293648 - lidocaine HCl 2 % with epinephrine 1:100,000 1.7 ML Dental Cartridge

* 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".