Desflurane Liquid
NDC Package 0781-6172-86

View Billable Units, 11-Digit Conversion Format, and RxNorm mappings
Table of Contents
    1. Package Information
    2. Frequently Asked Questions

Package Information

Desflurane liquids is the use of Desflurane, USP, Liquid for Inhalation is contraindicated in the following conditions:Known or suspected genetic susceptibility to malignant hyperthermia.Patients in whom general anesthesia is contraindicated.Induction of anesthesia in pediatric patients.Patients with known sensitivity to Desflurane, USP, Liquid for Inhalation or to other halogenated agents [see Warnings and Precautions (5.5)]. This formulation utilizes a liquid delivery system. Marketed by Sandoz Inc., this product is identified by NDC 0781-6172 and is authorized under FDA application ANDA208234.

Identification & Billing

NDC Package Code
0781-6172-86
Package Description
6 BOTTLE, GLASS in 1 CARTON / 240 mL in 1 BOTTLE, GLASS (0781-6172-22)
Product Code
0781-6172
11-Digit Billing Format
00781617286
Billing Unit
ML - Billing unit of "milliliter" is used when a product is measured by its liquid volume.
RxNorm Crosswalk

Clinical Specifications

Proprietary Name
Desflurane
Non-Proprietary Name
Desflurane
Substance Name
Desflurane
Dosage Form
Liquid - A dosage form consisting of a pure chemical in its liquid1 state. This dosage form term should not be applied to solutions.
Administration Route
Respiratory (inhalation) - Administration within the respiratory tract by inhaling orally or nasally for local or systemic effect.
Active Ingredient(s)
DESFLURANE 240 mL/240mL
Pharmacologic Class
Usage Information
The use of Desflurane, USP, Liquid for Inhalation is contraindicated in the following conditions:Known or suspected genetic susceptibility to malignant hyperthermia.Patients in whom general anesthesia is contraindicated.Induction of anesthesia in pediatric patients.Patients with known sensitivity to Desflurane, USP, Liquid for Inhalation or to other halogenated agents [see Warnings and Precautions (5.5)] . Patients with a history of moderate to severe hepatic dysfunction following anesthesia with Desflurane, USP, Liquid for Inhalation or other halogenated agents and not otherwise explained [see Warnings and Precautions (5.5)] .

Regulatory & Marketing

Labeler Name
Sandoz Inc.
Product Type
Human Prescription Drug
FDA Application #
ANDA208234
Marketing Category
ANDA - A product marketed under an approved Abbreviated New Drug Application.
Start Marketing Date
02-26-2018
Listing Expiration
12-31-2026
Exclude Flag
N
Sample Package
No

Hierarchy Structure

Code Lineage

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 full disclaimer at the bottom of this page.

Frequently Asked Questions

What is the distribution configuration for this product package?

The code 0781-6172-86 identifies a specific commercial package of 6 bottle, glass in 1 carton / 240 ml in 1 bottle, glass (0781-6172-22) of Desflurane, a human prescription drug labeled by Sandoz Inc.. This liquid is formulated for respiratory (inhalation) use and contains desflurane as the active substance.

Is this product currently listed with the FDA?

Yes, this product is active and verified within the NDC Directory. It was introduced to the market by Sandoz Inc. on February 26, 2018. The current certification is valid through December 31, 2026.

How is this Sandoz Inc. product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 00781617286. Quantities are measured in per "ml or milliliter", products billed per milliliter are usually products measured by liquid volume.. The table below illustrates the segment conversion from the 10-digit labeler code to the 11-digit provider format.

11-Digit Code Conversion

Billing payers usually require a 5-4-2 segment configuration. Below is the conversion from the 10-digit package format to the 11-digit billing format:

10-Digit Format (4-4-2)
0781-6172-86
11-Digit CMS (5-4-2)
00781-6172-86

Note: The zero is added to the Labeler segment to maintain the 5-4-2 structure.