NDC 51662-1589 Lidocaine Hcl And Epi

View Dosage, Usage, Ingredients, Routes, UNII

Product Information

This product is EXCLUDED from the official NDC directory because the listing certification is expired.
NDC Product Code:
51662-1589
Proprietary Name:
Lidocaine Hcl And Epi
Product Type: [3]
EXPIRED PRODUCT and EXCLUDED from the NDC Directory
Labeler Name: [5]
Hf Acquisition Co Llc, Dba Healthfirst
Labeler Code:
51662
Start Marketing Date: [9]
07-31-2022
Listing Expiration Date: [11]
12-31-2024
Exclude Flag: [12]
E
Code Structure:
Code Navigator:

Product Packages

NDC Code 51662-1589-3

Package Description: 25 POUCH in 1 CASE / 1 VIAL, MULTI-DOSE in 1 POUCH (51662-1589-2) / 50 mL in 1 VIAL, MULTI-DOSE

Product Details

What is NDC 51662-1589?

The NDC code 51662-1589 is assigned by the FDA to the product Lidocaine Hcl And Epi which is product labeled by Hf Acquisition Co Llc, Dba Healthfirst. The product's dosage form is . The product is distributed in a single package with assigned NDC code 51662-1589-3 25 pouch in 1 case / 1 vial, multi-dose in 1 pouch (51662-1589-2) / 50 ml in 1 vial, multi-dose. 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 Hcl And Epi?

Xylocaine (lidocaine HCl) Injections are indicated for production of local or regional anesthesia by infiltration techniques such as percutaneous injection and intravenous regional anesthesia by peripheral nerve block techniques such as brachial plexus and intercostal and by central neural techniques such as lumbar and caudal epidural blocks, when the accepted procedures for these techniques as described in standard textbooks are observed.

Which are Lidocaine Hcl And Epi UNII Codes?

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

Which are Lidocaine Hcl And Epi 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 Hcl And Epi?

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: 1010751 - lidocaine HCl 1 % / EPINEPHrine 1:100,000 Injectable Solution
  • RxCUI: 1010751 - epinephrine 0.01 MG/ML / lidocaine hydrochloride 10 MG/ML Injectable Solution
  • RxCUI: 1010751 - epinephrine (as epinephrine bitartrate) 1:100,000 / lidocaine hydrochloride 1 % Injectable Solution

* 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".