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  5. NDC Package Code: 67262-2000-1 Dantrolene Sodium

NDC Package 67262-2000-1 Dantrolene Sodium

Powder - View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. Frequently Asked Questions

Package Information

This product is an UNFINISHED DRUG part of the official NDC directory. Unfinished drugs include products like active ingredients some of which are used in bulk for further processing or compounding. The FDA requires a list of these drugs manufactured in a U.S. commercial distribution facility.

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:
67262-2000-1
Package Description:
4 kg in 1 DRUM
Product Code:
67262-2000
Non-Proprietary Name:
Dantrolene Sodium
Substance Name:
Dantrolene Sodium
Usage Information:
This medication is used to treat muscle tightness and cramping (spasms) caused by certain nerve disorders such as spinal cord injury, stroke, cerebral palsy, and multiple sclerosis. It works by relaxing the muscles. Dantrolene helps reduce muscle pain and stiffness, improves your ability to move around, and lets you do more of your daily activities. Dantrolene is also used with other treatments to prevent or treat special cases of high fever (malignant hyperthermia) related to anesthesia and surgery.
11-Digit NDC Billing Format:
67262200001
Product Type:
Bulk Ingredient
Labeler Name:
Has Healthcare Advanced Synthesis Sa
Dosage Form:
Powder - An intimate mixture of dry, finely divided drugs and/or chemicals that may be intended for internal or external use.
Active Ingredient(s):
  • DANTROLENE SODIUM 1 kg/kg
    • Sample Package:
    N/A
    Marketing Category:
    BULK INGREDIENT - A category specifying that a product is marketed as a bulk ingredient.
    Start Marketing Date:
    10-01-2007
    Listing Expiration Date:
    12-31-2024
    Exclude Flag:
    N
    Unfinished Product:
    Yes
    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 67262-2000-1?

    The NDC Packaged Code 67262-2000-1 is assigned to an UNFINISHED drug package of 4 kg in 1 drum of Dantrolene Sodium, a bulk ingredient labeled by Has Healthcare Advanced Synthesis Sa. The product's dosage form is powder and is administered via form.

    Is NDC 67262-2000 included in the NDC Directory?

    Yes, Dantrolene Sodium is an UNFINISHED PRODUCT with code 67262-2000 that is active and included in the NDC Directory. The product was first marketed by Has Healthcare Advanced Synthesis Sa on October 01, 2007 and its listing in the NDC Directory is set to expire on December 31, 2024 if the product is not updated or renewed by the manufacturer.

    What is the 11-digit format for NDC 67262-2000-1?

    The 11-digit format is 67262200001. 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
    5-4-167262-2000-15-4-267262-2000-01