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  5. NDC Package Code: 69877-017-01 Ascorbic Acid

NDC Package 69877-017-01 Ascorbic Acid

View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. Frequently Asked Questions

Package Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.

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:
69877-017-01
Package Description:
1 VIAL, DISPENSING in 1 BOX / 50 mL in 1 VIAL, DISPENSING
Product Code:
69877-017
Proprietary Name:
Ascorbic Acid
Usage Information:
Ascorbic acid is recommended for the prevention and treatment of scurvy. Its parenteral administration is desirable for patients with an acute deficiency or for those whose absorption of orally ingested ascorbic acid is uncertain.Symptoms of mild deficiency may include faulty bone and tooth development, gingivitis, bleeding gums, and loosened teeth. Febrile states, chronic illness, and infection (pneumonia, whooping cough, tuberculosis, diphtheria, sinusitis, rheumatic fever, etc.) increases the need for ascorbic acid. Hemovascular disorders, burns, delayed fracture and wound healing are indications for an increase in the daily intake.
11-Digit NDC Billing Format:
69877001701
NDC to RxNorm Crosswalk:
  • RxCUI: 308395 - ascorbic acid 500 MG/ML Injectable Solution
  • RxCUI: 308395 - vitamin C 500 MG/ML Injectable Solution
  • RxCUI: 308395 - vit-C 500 MG/ML Injectable Solution
    • Labeler Name:
    Raw Materials International Overseas Llc
    Sample Package:
    No
    Start Marketing Date:
    07-02-2015
    Listing Expiration Date:
    12-31-2018
    Exclude Flag:
    I
    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 69877-017-01?

    The NDC Packaged Code 69877-017-01 is assigned to a package of 1 vial, dispensing in 1 box / 50 ml in 1 vial, dispensing of Ascorbic Acid, labeled by Raw Materials International Overseas Llc. The product's dosage form is and is administered via form.

    Is NDC 69877-017 included in the NDC Directory?

    No, Ascorbic Acid with product code 69877-017 is excluded from the NDC Directory because it's listing has been INACTIVATED by FDA. The product was first marketed by Raw Materials International Overseas Llc on July 02, 2015 and its listing in the NDC Directory is set to expire on December 31, 2018 if the product is not updated or renewed by the manufacturer.

    What is the 11-digit format for NDC 69877-017-01?

    The 11-digit format is 69877001701. 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
    5-3-269877-017-015-4-269877-0017-01