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  5. NDC Package Code: 0143-9192-01 Foscarnet Sodium

NDC Package 0143-9192-01 Foscarnet Sodium

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

Table of Contents

    1. Package Information
    2. 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:
0143-9192-01
Package Description:
10 CARTON in 1 CASE / 1 BOTTLE in 1 CARTON / 250 mL in 1 BOTTLE
Product Code:
0143-9192
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:
00143919201
NDC to RxNorm Crosswalk:
  • RxCUI: 1734377 - foscarnet sodium 6000 MG in 250 ML Injection
  • RxCUI: 1734377 - 250 ML foscarnet sodium 24 MG/ML Injection
  • RxCUI: 1734377 - foscarnet sodium 6000 MG per 250 ML Injection
    • Product Type:
    Human Prescription Drug
    Labeler Name:
    Hikma Pharmaceuticals Usa 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):
  • Chelating Activity - [MoA] (Mechanism of Action)
  • DNA Polymerase Inhibitors - [MoA] (Mechanism of Action)
  • Pyrophosphate Analog DNA Polymerase Inhibitor - [EPC] (Established Pharmacologic Class)
  • Pyrophosphate Analog - [EXT]
    • Sample Package:
    No
    FDA Application Number:
    ANDA213987
    Marketing Category:
    ANDA - A product marketed under an approved Abbreviated New Drug Application.
    Start Marketing Date:
    11-29-2023
    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.

    Frequently Asked Questions

    What is NDC 0143-9192-01?

    The NDC Packaged Code 0143-9192-01 is assigned to a package of 10 carton in 1 case / 1 bottle in 1 carton / 250 ml in 1 bottle of Foscarnet Sodium, a human prescription drug labeled by Hikma Pharmaceuticals Usa Inc.. The product's dosage form is injection, solution and is administered via intravenous form.

    Is NDC 0143-9192 included in the NDC Directory?

    Yes, Foscarnet Sodium with product code 0143-9192 is active and included in the NDC Directory. The product was first marketed by Hikma Pharmaceuticals Usa Inc. on November 29, 2023 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 0143-9192-01?

    The 11-digit format is 00143919201. 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 4-4-2 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
    4-4-20143-9192-015-4-200143-9192-01