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  5. NDC Package Code: 70518-1285-1 Pentoxifylline

NDC Package 70518-1285-1 Pentoxifylline

Tablet, Extended Release 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:
70518-1285-1
Package Description:
30 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
Product Code:
70518-1285
Proprietary Name:
Pentoxifylline
Non-Proprietary Name:
Pentoxifylline
Substance Name:
Pentoxifylline
Usage Information:
This medication is used to improve the symptoms of a certain blood flow problem in the legs/arms (intermittent claudication due to occlusive artery disease). Pentoxifylline can decrease the muscle aching/pain/cramps during exercise, including walking, that occur with intermittent claudication. Pentoxifylline belongs to a class of drugs known as hemorrheologic agents. It works by helping blood flow more easily through narrowed arteries. This increases the amount of oxygen that can be delivered by the blood when the muscles need more (such as during exercise) thereby increasing walking distance and duration.
11-Digit NDC Billing Format:
70518128501
NDC to RxNorm Crosswalk:
  • RxCUI: 312301 - pentoxifylline 400 MG Extended Release Oral Tablet
    • Product Type:
    Human Prescription Drug
    Labeler Name:
    Remedyrepack Inc.
    Dosage Form:
    Tablet, Extended Release - A solid dosage form containing a drug which allows at least a reduction in dosing frequency as compared to that drug presented in conventional dosage form.
    Administration Route(s):
  • Oral - Administration to or by way of the mouth.
    • Active Ingredient(s):
  • PENTOXIFYLLINE 400 mg/1
    • Pharmacologic Class(es):
  • Blood Viscosity Reducer - [EPC] (Established Pharmacologic Class)
  • Hematologic Activity Alteration - [PE] (Physiologic Effect)
    • Sample Package:
    No
    FDA Application Number:
    ANDA075191
    Marketing Category:
    ANDA - A product marketed under an approved Abbreviated New Drug Application.
    Start Marketing Date:
    07-06-2018
    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 70518-1285-1?

    The NDC Packaged Code 70518-1285-1 is assigned to a package of 30 tablet, extended release in 1 blister pack of Pentoxifylline, a human prescription drug labeled by Remedyrepack Inc.. The product's dosage form is tablet, extended release and is administered via oral form.

    Is NDC 70518-1285 included in the NDC Directory?

    Yes, Pentoxifylline with product code 70518-1285 is active and included in the NDC Directory. The product was first marketed by Remedyrepack Inc. on July 06, 2018 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 70518-1285-1?

    The 11-digit format is 70518128501. 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
    5-4-170518-1285-15-4-270518-1285-01