Phenobarbital Sodium Injection, Solution
NDC Package 14789-128-05

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

Package Information

Phenobarbital Sodium injection is barbiturates are contraindicated in patients with known barbiturate sensitivity. This formulation utilizes a injection, solution delivery system. Marketed by Nexus Pharmaceuticals, Llc, this product is identified by NDC 14789-128.

Identification & Billing

NDC Package Code
14789-128-05
Package Description
10 VIAL, GLASS in 1 CARTON / 1 mL in 1 VIAL, GLASS (14789-128-07)
Product Code
14789-128
11-Digit Billing Format
14789012805
Billing Unit
ML - Billing unit of "milliliter" is used when a product is measured by its liquid volume.
RxNorm Crosswalk

Clinical Specifications

Proprietary Name
Phenobarbital Sodium
Non-Proprietary Name
Phenobarbital Sodium
Substance Name
Phenobarbital Sodium
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
  • Intramuscular - Administration within a muscle.
  • Intravenous - Administration within or into a vein or veins.
Active Ingredient(s)
PHENOBARBITAL SODIUM 130 mg/mL
Usage Information
Barbiturates are contraindicated in patients with known barbiturate sensitivity. Barbiturates are also contraindicated in patients with a history of manifest or latent porphyria, marked impairment of liver functions or with severe respiratory distress where dyspnea or obstruction is evident. Large doses are contraindicated in nephritic subjects. Barbiturates should not be administered to persons with known previous addiction to the sedative hypnotic group since ordinary doses may be ineffectual and may contribute to further addiction. Intraarterial administration is contraindicated. Its consequences vary from transient pain to gangrene. Subcutaneous administration produces tissue irritation, ranging from tenderness and redness to necrosis and is not recommended. (See DOSAGE AND ADMINISTRATION, Treatment of Adverse Effects Due to Inadvertent Error in Administration.)
DEA Schedule
Schedule IV (CIV) Substances

Regulatory & Marketing

Labeler Name
Nexus Pharmaceuticals, Llc
Product Type
Human Prescription Drug
Marketing Category
UNAPPROVED DRUG OTHER - An unapproved drug product in a marketing category that is not reflected on a particular list.
Start Marketing Date
12-06-2023
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.

Billing & HCPCS Mapping

To facilitate insurance claims and reimbursement, this drug package is mapped to specific HCPCS administrative codes. This crosswalk aligns clinical data with the billing standards used in ASP (Average Sales Price), AWP, and OPPS payment systems. Use the cards below to identify the correct billable units for provider claims.

J2560
Source: PDAC
INJECTION, PHENOBARBITAL SODIUM, UP TO 120 MG
HCPCS Dosage 120 MG
Units / Pkg

Note for Medical Coders: These mappings are synthesized from various CMS datasets including OPPS, PrEP, and DAC (Data Analysis and Coding) contractors. Always confirm unit conversions against the current quarter's pricing files before final submission.

* 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 14789-128-05 identifies a specific commercial package of 10 vial, glass in 1 carton / 1 ml in 1 vial, glass (14789-128-07) of Phenobarbital Sodium, a human prescription drug labeled by Nexus Pharmaceuticals, Llc. This injection, solution is formulated for intramuscular; intravenous use and contains phenobarbital sodium 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 Nexus Pharmaceuticals, Llc on December 06, 2023. The current certification is valid through December 31, 2026.

How is this Nexus Pharmaceuticals, Llc product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 14789012805. 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 (5-3-2)
14789-128-05
11-Digit CMS (5-4-2)
14789-0128-05

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