NDC Package 44567-662-10 Diltiazem Hydrochloride In Sodium Chloride

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

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:
44567-662-10
Package Description:
10 BAG in 1 CARTON / 100 mL in 1 BAG (44567-662-01)
Product Code:
Proprietary Name:
Diltiazem Hydrochloride In Sodium Chloride
Non-Proprietary Name:
Diltiazem Hydrochloride
Substance Name:
Diltiazem Hydrochloride
Usage Information:
Diltiazem Hydrochloride in Sodium Chloride Injection is contraindicated in the following situations: •Patients with sick sinus syndrome or second- or third-degree AV block except in the presence of a functioning ventricular pacemaker. •Patients with severe hypotension or cardiogenic shock. •Patients who have demonstrated hypersensitivity to the drug.• Concomitant administration with IV beta-blockers.•Patients with atrial fibrillation or atrial flutter associated with an accessory bypass tract such as in WPW syndrome.•Patients with ventricular tachycardia.
11-Digit NDC Billing Format:
44567066210
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:
Wg Critical Care, Llc
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):
Sample Package:
No
FDA Application Number:
NDA218038
Marketing Category:
NDA - A product marketed under an approved New Drug Application.
Start Marketing Date:
03-21-2025
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.

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Frequently Asked Questions

What is NDC 44567-662-10?

The NDC Packaged Code 44567-662-10 is assigned to a package of 10 bag in 1 carton / 100 ml in 1 bag (44567-662-01) of Diltiazem Hydrochloride In Sodium Chloride, a human prescription drug labeled by Wg Critical Care, Llc. The product's dosage form is injection, solution and is administered via intravenous form.

Is NDC 44567-662 included in the NDC Directory?

Yes, Diltiazem Hydrochloride In Sodium Chloride with product code 44567-662 is active and included in the NDC Directory. The product was first marketed by Wg Critical Care, Llc on March 21, 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 NDC billing unit for package 44567-662-10?

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 44567-662-10?

The 11-digit format is 44567066210. 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
5-3-244567-662-105-4-244567-0662-10