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  5. NDC Package Code: 51662-1317-3 6% Hetastarch In 0.9% Sodium Chloride

NDC Package 51662-1317-3 6% Hetastarch In 0.9% Sodium Chloride

Injection, Solution Intravenous - View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. Other Packages
    3. Frequently Asked Questions

Package Information

Find all the important details about this NDC Package code, including the 11-Digit NDC Billing number, billing units, wholesale price, RxNorm crosswalk, active ingredients, pharmacologic clasess, etc.

NDC Package Code:
51662-1317-3
Package Description:
12 CONTAINER in 1 CASE / 500 mL in 1 CONTAINER (51662-1317-2)
Product Code:
51662-1317
Proprietary Name:
6% Hetastarch In 0.9% Sodium Chloride
Non-Proprietary Name:
6% Hetastarch In 0.9% Sodium Chloride
Substance Name:
Hetastarch
Usage Information:
6% Hetastarch in 0.9% Sodium Chloride Injection is indicated in the treatment of hypovolemia when plasma volume expansion is desired. It is not a substitute for blood or plasma.The adjunctive use of 6% Hetastarch in 0.9% Sodium Chloride Injection in leukapheresis has also been shown to be safe and efficacious in improving the harvesting and increasing the yield of granulocytes by centrifugal means.
11-Digit NDC Billing Format:
51662131703
NDC to RxNorm Crosswalk:
  • RxCUI: 310757 - hetastarch 6 % in 500 ML Injection
  • RxCUI: 310757 - 500 ML hetastarch 60 MG/ML Injection
  • RxCUI: 310757 - hetastarch 6 % per 500 ML Injection
    • Product Type:
    Human Prescription Drug
    Labeler Name:
    Hf Acquisition Co Llc, Dba Healthfirst
    Dosage Form:
    Injection, Solution - A liquid preparation containing one or more drug substances dissolved in a suitable solvent or mixture of mutually miscible solvents that is suitable for injection.
    Administration Route(s):
  • Intravenous - Administration within or into a vein or veins.
    • Active Ingredient(s):
  • HETASTARCH 6 g/100mL
    • Pharmacologic Class(es):
  • Increased Intravascular Volume - [PE] (Physiologic Effect)
  • Osmotic Activity - [MoA] (Mechanism of Action)
  • Plasma Volume Expander - [EPC] (Established Pharmacologic Class)
  • Starch - [CS]
    • Sample Package:
    No
    FDA Application Number:
    BA740193
    Marketing Category:
    ANDA - A product marketed under an approved Abbreviated New Drug Application.
    Start Marketing Date:
    11-26-2018
    Listing Expiration Date:
    12-31-2025
    Exclude Flag:
    N
    Code Structure:

    The NDC Directory contains ONLY information on final marketed drugs submitted to FDA electronically by labelers. A labeler might be a manufacturer, re-packager or re-labeler. The product information included in the NDC directory does not indicate that FDA has verified the information provided by the product labeler. Assigned NDC numbers are not in any way an indication of FDA approval of the product.

    * Please review the disclaimer below.

    Other Product Packages

    The following packages are also available for this product:

    NDC Package CodePackage Description
    51662-1317-1500 mL in 1 CONTAINER

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 51662-1317-3?

    The NDC Packaged Code 51662-1317-3 is assigned to a package of 12 container in 1 case / 500 ml in 1 container (51662-1317-2) of 6% Hetastarch In 0.9% Sodium Chloride, a human prescription drug labeled by Hf Acquisition Co Llc, Dba Healthfirst. The product's dosage form is injection, solution and is administered via intravenous form.

    Is NDC 51662-1317 included in the NDC Directory?

    Yes, 6% Hetastarch In 0.9% Sodium Chloride with product code 51662-1317 is active and included in the NDC Directory. The product was first marketed by Hf Acquisition Co Llc, Dba Healthfirst on November 26, 2018 and its listing in the NDC Directory is set to expire on December 31, 2025 if the product is not updated or renewed by the manufacturer.

    What is the 11-digit format for NDC 51662-1317-3?

    The 11-digit format is 51662131703. The 11-digit billing format might be required by the Centers for Medicare & Medicaid Services (CMS) and other payers in billing claim forms.

    This package code is originally configured in a 5-4-1 segment 10-digit format and by adding a zero within the original NDC package code we can obtain the converted 11-digit format in a 5-4-2 segment configuration. The table below shows the 11-digit code conversion:

    10-Digit Format10-Digit Original Code11-Digit Format11-Digit Code
    5-4-151662-1317-35-4-251662-1317-03