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  4. NDC Product Code: 70529-024 Nacellate Solution 0.9% - 1000ml

NDC 70529-024 Nacellate Solution 0.9% - 1000ml

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 70529-024?
  4. Nacellate Solution 0.9% - 1000ml 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:
70529-024
Proprietary Name:
Nacellate Solution 0.9% - 1000ml
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
It3 Medical Llc
Labeler Code:
70529
Product Label ID:
14d1173d-d43c-4e7e-a945-35a5d612da19
Start Marketing Date: [9]
03-01-2017
Listing Expiration Date: [11]
12-31-2023
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 70529-024-01

Package Description: 1 BAG in 1 PACKAGE / 1000 mL in 1 BAG

Product Details

What is NDC 70529-024?

The NDC code 70529-024 is assigned by the FDA to the product Nacellate Solution 0.9% - 1000ml which is product labeled by It3 Medical Llc. The product's dosage form is . The product is distributed in a single package with assigned NDC code 70529-024-01 1 bag in 1 package / 1000 ml in 1 bag. 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 Nacellate Solution 0.9% - 1000ml?

Sodium Chloride Injection, USP is indicated as a source of water and electrolytes.0.9% Sodium Chloride Injection, USP is also indicated for use as a priming solution in hemodialysis procedures.

Which are Nacellate Solution 0.9% - 1000ml UNII Codes?

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

Which are Nacellate Solution 0.9% - 1000ml 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 Nacellate Solution 0.9% - 1000ml?

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

[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".