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

View Billable Units, 11-Digit Conversion Format, and RxNorm mappings
Table of Contents
    1. Package Information
    2. Other Packages
    3. Frequently Asked Questions

Package Information

6% Hetastarch In 0.9% Sodium Chloride injection is indicated in the treatment of hypovolemia when plasma volume expansion is desired. This formulation utilizes a injection, solution delivery system. Marketed by Hf Acquisition Co Llc, Dba Healthfirst, this product is identified by NDC 51662-1317 and is authorized under FDA application BA740193.

Identification & Billing

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
11-Digit Billing Format
51662131703
RxNorm Crosswalk

Clinical Specifications

Proprietary Name
6% Hetastarch In 0.9% Sodium Chloride
Non-Proprietary Name
6% Hetastarch In 0.9% Sodium Chloride
Substance Name
Hetastarch
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
Intravenous - Administration within or into a vein or veins.
Active Ingredient(s)
HETASTARCH 6 g/100mL
Pharmacologic Class
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.

Regulatory & Marketing

Labeler Name
Hf Acquisition Co Llc, Dba Healthfirst
Product Type
Human Prescription Drug
FDA Application #
BA740193
Marketing Category
ANDA - A product marketed under an approved Abbreviated New Drug Application.
Start Marketing Date
11-26-2018
Listing Expiration
12-31-2026
Exclude Flag
N
Sample Package
No

Hierarchy Structure

Code Lineage

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 full disclaimer at the bottom of this page.

Other Available Packages

The following commercial packages are registered under the same Product NDC (51662-1317). Click a package code to view its specific billing and regulatory data.

51662-1317-1
500 mL in 1 CONTAINER

* Please review the full disclaimer at the bottom of this page.

Frequently Asked Questions

What is the distribution configuration for this product package?

The code 51662-1317-3 identifies a specific commercial 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. This injection, solution is formulated for intravenous use and contains hetastarch as the active substance.

Is this product currently listed with the FDA?

Yes, this product is active and verified within the NDC Directory. It was introduced to the market by Hf Acquisition Co Llc, Dba Healthfirst on November 26, 2018. The current certification is valid through December 31, 2026.

How is this Hf Acquisition Co Llc, Dba Healthfirst product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 51662131703. The table below illustrates the segment conversion from the 10-digit labeler code to the 11-digit provider format.

11-Digit Code Conversion

Billing payers usually require a 5-4-2 segment configuration. Below is the conversion from the 10-digit package format to the 11-digit billing format:

10-Digit Format (5-4-1)
51662-1317-3
11-Digit CMS (5-4-2)
51662-1317-03

Note: The zero is added to the Package segment to maintain the 5-4-2 structure.