NDC Package 69575-4036-2 Dantrolene Sodium

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

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:
69575-4036-2
Package Description:
30 kg in 1 DRUM
Product Code:
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:
69575403602
Product Type:
Bulk Ingredient
Labeler Name:
Azico Biophore India Private Limited
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):
Sample Package:
N/A
Marketing Category:
BULK INGREDIENT - A category specifying that a product is marketed as a bulk ingredient.
Start Marketing Date:
10-29-2021
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.

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Frequently Asked Questions

What is NDC 69575-4036-2?

The NDC Packaged Code 69575-4036-2 is assigned to an UNFINISHED drug package of 30 kg in 1 drum of Dantrolene Sodium, a bulk ingredient labeled by Azico Biophore India Private Limited. The product's dosage form is powder and is administered via form.

Is NDC 69575-4036 included in the NDC Directory?

Yes, Dantrolene Sodium is an UNFINISHED PRODUCT with code 69575-4036 that is active and included in the NDC Directory. The product was first marketed by Azico Biophore India Private Limited on October 29, 2021 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 69575-4036-2?

The 11-digit format is 69575403602. 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
5-4-169575-4036-25-4-269575-4036-02