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  4. NDC Product Code: 85160-200 Turkfleks %0.9 Sodium Chloride

NDC 85160-200 Turkfleks %0.9 Sodium Chloride

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 85160-200?
  4. Turkfleks %0.9 Sodium Chloride 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 certification is expired.

Get all the details for National Drug Code (NDC) 85160-200 in one place. This page breaks down everything you need to know about the NDC, including proprietary name, active and inactive substances, package configurations, billing units, labeler information, and routes of administration. It also includes enhanced data such as HCPCS codes, FDA product labels with images, UNIIs, and RxNorm cross-references. Whether you're a healthcare professional verifying drug data or a consumer researching medication, this NDC page helps you make informed, accurate decisions.

NDC Product Code:
85160-200
Proprietary Name:
Turkfleks %0.9 Sodium Chloride
Product Type: [3]
EXPIRED PRODUCT and EXCLUDED from the NDC Directory
Labeler Name: [5]
Turk Ilac Ve Serum Sanayi Anonim Sirketi
Labeler Code:
85160
Product Label ID:
3170d1ee-c6c9-5c35-e063-6294a90a5f04
Marketing Category: [8]
UNAPPROVED DRUG FOR USE IN DRUG SHORTAGE -
Start Marketing Date: [9]
01-15-2025
Listing Expiration Date: [11]
12-31-2026
Exclude Flag: [12]
E
Code Navigator:

Code Structure Chart

Product Details

What is NDC 85160-200?

The NDC code 85160-200 is assigned by the FDA to the product Turkfleks %0.9 Sodium Chloride which is product labeled by Turk Ilac Ve Serum Sanayi Anonim Sirketi. The product's dosage form is . The product is distributed in 7 packages with assigned NDC codes 85160-200-10 100 bag in 1 box / 50 ml in 1 bag (85160-200-01), 85160-200-20 50 bag in 1 box / 100 ml in 1 bag (85160-200-02), 85160-200-30 50 bag in 1 box / 150 ml in 1 bag (85160-200-03), 85160-200-40 25 bag in 1 box / 250 ml in 1 bag (85160-200-04), 85160-200-50 20 bag in 1 box / 500 ml in 1 bag (85160-200-05), 85160-200-60 20 bag in 1 box / 1000 ml in 1 bag (85160-200-06), 85160-200-70 10 bag in 1 box / 3000 ml in 1 bag (85160-200-07). 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 Turkfleks %0.9 Sodium Chloride?

The solution is contraindicated in patients with hypernatremia or hyperchloremia. It should also not be used in cases where sodium or chloride administration is clinically harmful.

Which are Turkfleks %0.9 Sodium Chloride UNII Codes?

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

What is the NDC to RxNorm Crosswalk for Turkfleks %0.9 Sodium Chloride?

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.

[8] What is the Marketing Category? - Product types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.

[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, or because the listing certification is expired, or because the listing data was inactivated by FDA, or because it was discontinued by the labeler. Possible values in this field are: "D", "E", "I", "N", "U".