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  5. NDC Package Code: 23155-771-31 Foscarnet Sodium

NDC Package 23155-771-31 Foscarnet Sodium

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:
23155-771-31
Package Description:
1 BOTTLE, GLASS in 1 CARTON / 250 mL in 1 BOTTLE, GLASS
Product Code:
23155-771
Proprietary Name:
Foscarnet Sodium
Non-Proprietary Name:
Foscarnet Sodium
Substance Name:
Foscarnet Sodium
Usage Information:
Foscarnet sodium injection is contraindicated in patients with clinically significant hypersensitivity to foscarnet sodium.
11-Digit NDC Billing Format:
23155077131
Billing Unit:
ML - Billing unit of "milliliter" is used when a product is measured by its liquid volume.
NDC to RxNorm Crosswalk:
Product Type:
Human Prescription Drug
Labeler Name:
Heritage Pharmaceuticals Inc. D/b/a Avet Pharmaceuticals Inc.
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):
FOSCARNET SODIUM 24 mg/mL
Pharmacologic Class(es):
Sample Package:
No
FDA Application Number:
ANDA213807
Marketing Category:
ANDA - A product marketed under an approved Abbreviated New Drug Application.
Start Marketing Date:
06-05-2023
Listing Expiration Date:
12-31-2026
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
23155-771-4110 BOTTLE, GLASS in 1 CARTON / 250 mL in 1 BOTTLE, GLASS

* Please review the disclaimer below.

Frequently Asked Questions

What is NDC 23155-771-31?

The NDC Packaged Code 23155-771-31 is assigned to a package of 1 bottle, glass in 1 carton / 250 ml in 1 bottle, glass of Foscarnet Sodium, a human prescription drug labeled by Heritage Pharmaceuticals Inc. D/b/a Avet Pharmaceuticals Inc.. The product's dosage form is injection, solution and is administered via intravenous form.

Is NDC 23155-771 included in the NDC Directory?

Yes, Foscarnet Sodium with product code 23155-771 is active and included in the NDC Directory. The product was first marketed by Heritage Pharmaceuticals Inc. D/b/a Avet Pharmaceuticals Inc. on June 05, 2023 and its listing in the NDC Directory is set to expire on December 31, 2026 if the product is not updated or renewed by the manufacturer.

What is the NDC billing unit for package 23155-771-31?

The contents of this package are billed per "ml or milliliter", products billed per milliliter are usually products measured by liquid volume.

What is the 11-digit format for NDC 23155-771-31?

The 11-digit format is 23155077131. 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 5-3-2 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
5-3-223155-771-315-4-223155-0771-31