NDC Package 51754-2130-4 Midazolam 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:
51754-2130-4
Package Description:
25 VIAL in 1 CARTON / 50 mL in 1 VIAL
Product Code:
Proprietary Name:
Midazolam Hydrochloride
Non-Proprietary Name:
Midazolam Hydrochloride
Substance Name:
Midazolam Hydrochloride
Usage Information:
Midazolam in Sodium Chloride Injection is indicated:Continuous intravenous infusion for sedation of intubated and mechanically ventilated adult, pediatric, and neonatal patients as a component of anesthesia or during treatment in a critical care setting.
11-Digit NDC Billing Format:
51754213004
NDC to RxNorm Crosswalk:
  • RxCUI: 2541170 - midazolam 50 MG in 50 mL Injection
  • RxCUI: 2541170 - 50 ML midazolam 1 MG/ML Injection
  • RxCUI: 2541170 - midazolam 50 MG per 50 ML Injection
  • RxCUI: 2541171 - midazolam 100 MG in 100 mL Injection
  • RxCUI: 2541171 - 100 ML midazolam 1 MG/ML Injection
  • Product Type:
    Human Prescription Drug
    Labeler Name:
    Exela Pharma Sciences, 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):
    DEA Schedule:
    Schedule IV (CIV) Substances
    Sample Package:
    No
    FDA Application Number:
    NDA215868
    Marketing Category:
    NDA - A product marketed under an approved New Drug Application.
    Start Marketing Date:
    12-01-2022
    Listing Expiration Date:
    12-31-2024
    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.

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 51754-2130-4?

    The NDC Packaged Code 51754-2130-4 is assigned to a package of 25 vial in 1 carton / 50 ml in 1 vial of Midazolam Hydrochloride, a human prescription drug labeled by Exela Pharma Sciences, Llc. The product's dosage form is injection, solution and is administered via intravenous form.

    Is NDC 51754-2130 included in the NDC Directory?

    Yes, Midazolam Hydrochloride with product code 51754-2130 is active and included in the NDC Directory. The product was first marketed by Exela Pharma Sciences, Llc on December 01, 2022 and its listing in the NDC Directory is set to expire on December 31, 2024 if the product is not updated or renewed by the manufacturer.

    What is the 11-digit format for NDC 51754-2130-4?

    The 11-digit format is 51754213004. 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 5-4-1 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
    5-4-151754-2130-45-4-251754-2130-04