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  5. NDC Package Code: 51991-999-17 Dehydrated Alcohol

NDC Package 51991-999-17 Dehydrated Alcohol

Alcohol Injection, Solution Intra-arterial - 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:
51991-999-17
Package Description:
10 VIAL, GLASS in 1 CARTON / 5 mL in 1 VIAL, GLASS (51991-999-75)
Product Code:
51991-999
Proprietary Name:
Dehydrated Alcohol
Non-Proprietary Name:
Alcohol
Substance Name:
Alcohol
Usage Information:
Dehydrated alcohol injection is indicated to induce controlled cardiac septal infarction to improve exercise capacity in adults with symptomatic hypertrophic obstructive cardiomyopathy who are not candidates for surgical myectomy.
11-Digit NDC Billing Format:
51991099917
Product Type:
Human Prescription Drug
Labeler Name:
Breckenridge Pharmaceutical 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):
Intra-arterial - Administration within an artery or arteries.
Active Ingredient(s):
ALCOHOL 1 mL/mL
Sample Package:
No
FDA Application Number:
ANDA219444
Marketing Category:
ANDA - A product marketed under an approved Abbreviated New Drug Application.
Start Marketing Date:
09-23-2025
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.

Frequently Asked Questions

What is NDC 51991-999-17?

The NDC Packaged Code 51991-999-17 is assigned to a package of 10 vial, glass in 1 carton / 5 ml in 1 vial, glass (51991-999-75) of Dehydrated Alcohol, a human prescription drug labeled by Breckenridge Pharmaceutical Inc. The product's dosage form is injection, solution and is administered via intra-arterial form.

Is NDC 51991-999 included in the NDC Directory?

Yes, Dehydrated Alcohol with product code 51991-999 is active and included in the NDC Directory. The product was first marketed by Breckenridge Pharmaceutical Inc on September 23, 2025 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 11-digit format for NDC 51991-999-17?

The 11-digit format is 51991099917. 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
5-3-251991-999-175-4-251991-0999-17