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  5. NDC Package Code: 11704-650-10 Seizalam

NDC Package 11704-650-10 Seizalam

Midazolam Hydrochloride Injection, Solution Intramuscular - View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. Frequently Asked Questions

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:
11704-650-10
Package Description:
10 VIAL, GLASS in 1 CARTON / 10 mL in 1 VIAL, GLASS (11704-650-01)
Product Code:
11704-650
Proprietary Name:
Seizalam
Non-Proprietary Name:
Midazolam Hydrochloride
Substance Name:
Midazolam Hydrochloride
Usage Information:
Seizalam is indicated for the treatment of status epilepticus in adults.
11-Digit NDC Billing Format:
11704065010
NDC to RxNorm Crosswalk:
  • RxCUI: 2057964 - Seizalam 5 MG/ML Injectable Solution
  • RxCUI: 2057964 - midazolam 5 MG/ML Injectable Solution [Seizalam]
  • RxCUI: 311702 - midazolam 5 MG/ML Injectable Solution
  • RxCUI: 311702 - midazolam (as midazolam hydrochloride) 5 MG/ML Injectable Solution
    • Product Type:
    Human Prescription Drug
    Labeler Name:
    Meridian Medical Technologies 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):
  • Intramuscular - Administration within a muscle.
    • Active Ingredient(s):
  • MIDAZOLAM HYDROCHLORIDE 5 mg/mL
    • Pharmacologic Class(es):
  • Benzodiazepine - [EPC] (Established Pharmacologic Class)
  • Benzodiazepines - [CS]
    • DEA Schedule:
    Schedule IV (CIV) Substances
    Sample Package:
    No
    FDA Application Number:
    NDA209566
    Marketing Category:
    NDA - A product marketed under an approved New Drug Application.
    Start Marketing Date:
    09-14-2018
    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 11704-650-10?

    The NDC Packaged Code 11704-650-10 is assigned to a package of 10 vial, glass in 1 carton / 10 ml in 1 vial, glass (11704-650-01) of Seizalam, a human prescription drug labeled by Meridian Medical Technologies Llc. The product's dosage form is injection, solution and is administered via intramuscular form.

    Is NDC 11704-650 included in the NDC Directory?

    Yes, Seizalam with product code 11704-650 is active and included in the NDC Directory. The product was first marketed by Meridian Medical Technologies Llc on September 14, 2018 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 11704-650-10?

    The 11-digit format is 11704065010. 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 5-3-2 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
    5-3-211704-650-105-4-211704-0650-10