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  5. NDC Package Code: 70518-2358-1 Diazepam

NDC Package 70518-2358-1 Diazepam

Injection, Solution Intramuscular; Intravenous - 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:
70518-2358-1
Package Description:
10 SYRINGE, GLASS in 1 CARTON / 2 mL in 1 SYRINGE, GLASS (70518-2358-2)
Product Code:
70518-2358
Proprietary Name:
Diazepam
Non-Proprietary Name:
Diazepam
Substance Name:
Diazepam
Usage Information:
Diazepam is used to treat anxiety, alcohol withdrawal, and seizures. It is also used to relieve muscle spasms and to provide sedation before medical procedures. This medication works by calming the brain and nerves. Diazepam belongs to a class of drugs known as benzodiazepines.
11-Digit NDC Billing Format:
70518235801
NDC to RxNorm Crosswalk:
  • RxCUI: 2120550 - diazePAM 10 MG in 2 ML Prefilled Syringe
  • RxCUI: 2120550 - 2 ML diazepam 5 MG/ML Prefilled Syringe
  • RxCUI: 2120550 - diazepam 10 MG per 2 ML Prefilled Syringe
    • Product Type:
    Human Prescription Drug
    Labeler Name:
    Remedyrepack Inc.
    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):
  • DIAZEPAM 10 mg/2mL
    • Pharmacologic Class(es):
  • Benzodiazepine - [EPC] (Established Pharmacologic Class)
  • Benzodiazepines - [CS]
    • DEA Schedule:
    Schedule IV (CIV) Substances
    Sample Package:
    No
    FDA Application Number:
    ANDA210363
    Marketing Category:
    ANDA - A product marketed under an approved Abbreviated New Drug Application.
    Start Marketing Date:
    10-10-2019
    Listing Expiration Date:
    12-31-2025
    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 70518-2358-1?

    The NDC Packaged Code 70518-2358-1 is assigned to a package of 10 syringe, glass in 1 carton / 2 ml in 1 syringe, glass (70518-2358-2) of Diazepam, a human prescription drug labeled by Remedyrepack Inc.. The product's dosage form is injection, solution and is administered via intramuscular; intravenous form.

    Is NDC 70518-2358 included in the NDC Directory?

    Yes, Diazepam with product code 70518-2358 is active and included in the NDC Directory. The product was first marketed by Remedyrepack Inc. on October 10, 2019 and its listing in the NDC Directory is set to expire on December 31, 2025 if the product is not updated or renewed by the manufacturer.

    What is the 11-digit format for NDC 70518-2358-1?

    The 11-digit format is 70518235801. 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
    5-4-170518-2358-15-4-270518-2358-01