1. Home
  2. Labeler Index
  3. Sanovel Ilac San. Ve Tic.a.s.
  4. NDC Product Code: 71479-004 Rocuronium Bromide

NDC 71479-004 Rocuronium Bromide

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 71479-004?
  4. Rocuronium Bromide Uses
  5. Active Ingredients UNII Codes
  6. 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:
71479-004
Proprietary Name:
Rocuronium Bromide
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Sanovel Ilac San. Ve Tic.a.s.
Labeler Code:
71479
Product Label ID:
ba999c24-fe3c-4d8f-981f-17d8639bc16b
Start Marketing Date: [9]
12-31-2019
Listing Expiration Date: [11]
12-31-2020
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 71479-004-10

Package Description: 10 VIAL, MULTI-DOSE in 1 BOX / 10 mL in 1 VIAL, MULTI-DOSE

Product Details

What is NDC 71479-004?

The NDC code 71479-004 is assigned by the FDA to the product Rocuronium Bromide which is product labeled by Sanovel Ilac San. Ve Tic.a.s.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 71479-004-10 10 vial, multi-dose in 1 box / 10 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 Rocuronium Bromide?

Rocuronium bromide Injection is indicated for inpatients and outpatients as an adjunct to general anesthesia to facilitate both rapid sequence and routine tracheal intubation, and to provide skeletal muscle relaxation during surgery or mechanical ventilation.

Which are Rocuronium Bromide UNII Codes?

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

What is the NDC to RxNorm Crosswalk for Rocuronium Bromide?

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: 1234995 - rocuronium bromide 10 MG/ML Injectable Solution
  • RxCUI: 1234995 - rocuronium bromide 100 MG per 10 ML Concentrate for Injectable Solution
  • RxCUI: 1234995 - rocuronium bromide 50 MG per 5 ML Concentrate for 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".