Dexmedetomidine Hydrochloride In Sodium Chloride Injection, Solution
NDC Package 68094-047-10

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

Package Information

Dexmedetomidine Hydrochloride In Sodium Chloride (dexmedetomidine hydrochloride) injection is none. This formulation utilizes a injection, solution delivery system. Marketed by Precision Dose, Inc., this product is identified by NDC 68094-047 and is authorized under FDA application ANDA212857.

Identification & Billing

NDC Package Code
68094-047-10
Package Description
10 VIAL in 1 CARTON / 20 mL in 1 VIAL (68094-047-01)
Product Code
68094-047
11-Digit Billing Format
68094004710
RxNorm Crosswalk

Clinical Specifications

Proprietary Name
Dexmedetomidine Hydrochloride In Sodium Chloride
Non-Proprietary Name
Dexmedetomidine Hydrochloride
Substance Name
Dexmedetomidine Hydrochloride
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
Intravenous - Administration within or into a vein or veins.
Active Ingredient(s)
DEXMEDETOMIDINE HYDROCHLORIDE 4 ug/mL
Pharmacologic Class
Usage Information
None.

Regulatory & Marketing

Labeler Name
Precision Dose, Inc.
Product Type
Human Prescription Drug
FDA Application #
ANDA212857
Marketing Category
ANDA - A product marketed under an approved Abbreviated New Drug Application.
Start Marketing Date
11-23-2020
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 68094-047-10 identifies a specific commercial package of 10 vial in 1 carton / 20 ml in 1 vial (68094-047-01) of Dexmedetomidine Hydrochloride In Sodium Chloride, a human prescription drug labeled by Precision Dose, Inc.. This injection, solution is formulated for intravenous use and contains dexmedetomidine hydrochloride 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 Precision Dose, Inc. on November 23, 2020. The current certification is valid through December 31, 2026.

How is this Precision Dose, Inc. product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 68094004710. 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 (5-3-2)
68094-047-10
11-Digit CMS (5-4-2)
68094-0047-10

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