NDC Package 70518-3672-0 Methotrexate

Tablet Oral - 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:
70518-3672-0
Package Description:
30 TABLET in 1 BLISTER PACK
Product Code:
Proprietary Name:
Methotrexate
Non-Proprietary Name:
Methotrexate
Substance Name:
Methotrexate Sodium
Usage Information:
Methotrexate is used to treat certain types of cancer or to control severe psoriasis or rheumatoid arthritis that has not responded to other treatments. It may also be used to control juvenile rheumatoid arthritis. Methotrexate belongs to a class of drugs known as antimetabolites. It works by slowing or stopping the growth of cancer cells and suppressing the immune system. Early treatment of rheumatoid arthritis with more aggressive therapy such as methotrexate helps to reduce further joint damage and to preserve joint function.
11-Digit NDC Billing Format:
70518367200
NDC to RxNorm Crosswalk:
  • RxCUI: 105585 - methotrexate 2.5 MG Oral Tablet
  • RxCUI: 105585 - methotrexate 2.5 MG (as methotrexate sodium) Oral Tablet
  • Product Type:
    Human Prescription Drug
    Labeler Name:
    Remedyrepack Inc.
    Dosage Form:
    Tablet - A solid dosage form containing medicinal substances with or without suitable diluents.
    Administration Route(s):
  • Oral - Administration to or by way of the mouth.
  • Active Ingredient(s):
    Sample Package:
    No
    FDA Application Number:
    ANDA210454
    Marketing Category:
    ANDA - A product marketed under an approved Abbreviated New Drug Application.
    Start Marketing Date:
    03-06-2023
    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 70518-3672-0?

    The NDC Packaged Code 70518-3672-0 is assigned to a package of 30 tablet in 1 blister pack of Methotrexate, a human prescription drug labeled by Remedyrepack Inc.. The product's dosage form is tablet and is administered via oral form.

    Is NDC 70518-3672 included in the NDC Directory?

    Yes, Methotrexate with product code 70518-3672 is active and included in the NDC Directory. The product was first marketed by Remedyrepack Inc. on March 06, 2023 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 70518-3672-0?

    The 11-digit format is 70518367200. 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
    5-4-170518-3672-05-4-270518-3672-00