NDC Package 42571-414-87 Midazolam

Injection, Solution Intramuscular; 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:
42571-414-87
Package Description:
25 VIAL in 1 CARTON / 2 mL in 1 VIAL (42571-414-75)
Product Code:
Proprietary Name:
Midazolam
Non-Proprietary Name:
Midazolam
Substance Name:
Midazolam Hydrochloride
Usage Information:
This medication is used by people with epilepsy to treat a certain type of serious seizure that doesn't stop (seizure clusters). Midazolam belongs to a class of drugs known as benzodiazepines. It may work by increasing the effect of a certain substance in your body (GABA), which helps calm the brain and nerves.
11-Digit NDC Billing Format:
42571041487
NDC to RxNorm Crosswalk:
  • RxCUI: 1666798 - midazolam 2 MG in 2 ML Injection
  • RxCUI: 1666798 - 2 ML midazolam 1 MG/ML Injection
  • RxCUI: 1666798 - midazolam 2 MG per 2 ML Injection
  • RxCUI: 1666814 - midazolam 5 MG in 1 ML Injection
  • RxCUI: 1666814 - 1 ML midazolam 5 MG/ML Injection
  • Product Type:
    Human Prescription Drug
    Labeler Name:
    Micro Labs Limited
    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.
  • Intravenous - Administration within or into a vein or veins.
  • Active Ingredient(s):
    DEA Schedule:
    Schedule IV (CIV) Substances
    Sample Package:
    No
    FDA Application Number:
    ANDA217504
    Marketing Category:
    ANDA - A product marketed under an approved Abbreviated New Drug Application.
    Start Marketing Date:
    01-01-2024
    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 42571-414-87?

    The NDC Packaged Code 42571-414-87 is assigned to a package of 25 vial in 1 carton / 2 ml in 1 vial (42571-414-75) of Midazolam, a human prescription drug labeled by Micro Labs Limited. The product's dosage form is injection, solution and is administered via intramuscular; intravenous form.

    Is NDC 42571-414 included in the NDC Directory?

    Yes, Midazolam with product code 42571-414 is active and included in the NDC Directory. The product was first marketed by Micro Labs Limited on January 01, 2024 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 42571-414-87?

    The 11-digit format is 42571041487. 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
    5-3-242571-414-875-4-242571-0414-87