Esmolol Hydrochloride Injection
NDC Package 71872-7136-1

View Billable Units, 11-Digit Conversion Format, and RxNorm mappings

Package Information

Esmolol Hydrochloride injection is this dosage form is prediluted to provide a ready-to-use, iso-osmotic solution of 10 mg/mL esmolol hydrochloride in sodium chloride recommended for esmolol hydrochloride intravenous administration. This formulation utilizes a injection delivery system. Marketed by Medical Purchasing Solutions, Llc, this product is identified by NDC 71872-7136 and is authorized under FDA application NDA019386.

Identification & Billing

NDC Package Code
71872-7136-1
Package Description
1 VIAL in 1 BAG / 10 mL in 1 VIAL
Product Code
11-Digit Billing Format
71872713601
RxNorm Crosswalk

Clinical Specifications

Proprietary Name
Esmolol Hydrochloride
Non-Proprietary Name
Esmolol Hydrochloride
Substance Name
Esmolol Hydrochloride
Dosage Form
Injection - A sterile preparation intended for parenteral use; five distinct classes of injections exist as defined by the USP.
Administration Route
Intravenous - Administration within or into a vein or veins.
Active Ingredient(s)
Usage Information
This dosage form is prediluted to provide a ready-to-use, iso-osmotic solution of 10 mg/mL esmolol hydrochloride in sodium chloride recommended for esmolol hydrochloride intravenous administration. The ready-to-use vial may be used to administer a loading dosage by hand-held syringe while the maintenance infusion is being prepared.When using a 10 mg/mL concentration, a loading dose of 0.5 mg/kg infused over 1 minute, for a 70 kg patient is 3.5 mL.Esmolol hydrochloride injection is not compatible with Sodium Bicarbonate (5%) solution (limited stability) or furosemide (precipitation).Parenteral drug products should be inspected visually for particulate matter and discoloration prior to administration, whenever solution and container permit.

Regulatory & Marketing

Labeler Name
Medical Purchasing Solutions, Llc
Product Type
Human Prescription Drug
FDA Application #
NDA019386
Marketing Category
NDA - A product marketed under an approved New Drug Application.
Start Marketing Date
12-31-1986
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 71872-7136-1 identifies a specific commercial package of 1 vial in 1 bag / 10 ml in 1 vial of Esmolol Hydrochloride, a human prescription drug labeled by Medical Purchasing Solutions, Llc. This injection is formulated for intravenous use and contains esmolol 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 Medical Purchasing Solutions, Llc on December 31, 1986. The current certification is valid through December 31, 2026.

How is this Medical Purchasing Solutions, Llc product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 71872713601. 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 (5-4-1)
71872-7136-1
11-Digit CMS (5-4-2)
71872-7136-01

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