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  5. NDC Package Code: 70518-1838-0 Mirtazapine

NDC Package 70518-1838-0 Mirtazapine

Tablet, Film Coated Oral - 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:
70518-1838-0
Package Description:
30 TABLET, FILM COATED in 1 BLISTER PACK
Product Code:
70518-1838
Proprietary Name:
Mirtazapine
Non-Proprietary Name:
Mirtazapine
Substance Name:
Mirtazapine
Usage Information:
Mirtazapine is used to treat depression. It improves mood and feelings of well-being. Mirtazapine is an antidepressant that works by restoring the balance of natural chemicals (neurotransmitters) in the brain.
11-Digit NDC Billing Format:
70518183800
NDC to RxNorm Crosswalk:
  • RxCUI: 311725 - mirtazapine 15 MG Oral Tablet
    • Product Type:
    Human Prescription Drug
    Labeler Name:
    Remedyrepack Inc.
    Dosage Form:
    Tablet, Film Coated - A solid dosage form that contains medicinal substances with or without suitable diluents and is coated with a thin layer of a water-insoluble or water-soluble polymer.
    Administration Route(s):
  • Oral - Administration to or by way of the mouth.
    • Active Ingredient(s):
  • MIRTAZAPINE 15 mg/1
    • Sample Package:
    No
    FDA Application Number:
    ANDA076921
    Marketing Category:
    ANDA - A product marketed under an approved Abbreviated New Drug Application.
    Start Marketing Date:
    01-30-2019
    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 70518-1838-0?

    The NDC Packaged Code 70518-1838-0 is assigned to a package of 30 tablet, film coated in 1 blister pack of Mirtazapine, a human prescription drug labeled by Remedyrepack Inc.. The product's dosage form is tablet, film coated and is administered via oral form.

    Is NDC 70518-1838 included in the NDC Directory?

    Yes, Mirtazapine with product code 70518-1838 is active and included in the NDC Directory. The product was first marketed by Remedyrepack Inc. on January 30, 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 70518-1838-0?

    The 11-digit format is 70518183800. 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
    5-4-170518-1838-05-4-270518-1838-00