NDC Package 70518-0763-0 Neomycin And Polymyxin B Sulfates And Hydrocortisone

Neomycin Sulfate,Polymyxin B Sulfate,Hydrocortisone Solution/ Drops Auricular (otic) - 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:
70518-0763-0
Package Description:
1 BOTTLE, DROPPER in 1 CARTON / 10 mL in 1 BOTTLE, DROPPER
Product Code:
Proprietary Name:
Neomycin And Polymyxin B Sulfates And Hydrocortisone
Non-Proprietary Name:
Neomycin Sulfate, Polymyxin B Sulfate, Hydrocortisone
Substance Name:
Hydrocortisone; Neomycin Sulfate; Polymyxin B Sulfate
Usage Information:
For the treatment of superficial bacterial infections of the external auditory canal caused by organisms susceptible to the action of the antibiotics.
11-Digit NDC Billing Format:
70518076300
NDC to RxNorm Crosswalk:
  • RxCUI: 204423 - neomycin sulfate 0.35 % / polymyxin B sulfate 10,000 UNT/ML / hydrocortisone 1 % Otic Solution
  • RxCUI: 204423 - hydrocortisone 10 MG/ML / neomycin 3.5 MG/ML / polymyxin B 10000 UNT/ML Otic Solution
  • RxCUI: 204423 - hydrocortisone 1 % / neomycin (as neomycin sulfate) 0.35 % / polymyxin B (as polymyxin B sulfate) 10,000 UNT/ML Otic Solution
  • RxCUI: 204423 - hydrocortisone 10 MG / neomycin 3.5 MG / polymyxin B 10,000 UNT per ML Otic Solution
  • Product Type:
    Human Prescription Drug
    Labeler Name:
    Remedyrepack Inc.
    Dosage Form:
    Solution/ Drops - A solution which is usually administered in a drop-wise fashion.
    Administration Route(s):
  • Auricular (otic) - Administration to or by way of the ear.
  • Sample Package:
    No
    FDA Application Number:
    ANDA064053
    Marketing Category:
    ANDA - A product marketed under an approved Abbreviated New Drug Application.
    Start Marketing Date:
    10-06-2017
    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 70518-0763-0?

    The NDC Packaged Code 70518-0763-0 is assigned to a package of 1 bottle, dropper in 1 carton / 10 ml in 1 bottle, dropper of Neomycin And Polymyxin B Sulfates And Hydrocortisone, a human prescription drug labeled by Remedyrepack Inc.. The product's dosage form is solution/ drops and is administered via auricular (otic) form.

    Is NDC 70518-0763 included in the NDC Directory?

    Yes, Neomycin And Polymyxin B Sulfates And Hydrocortisone with product code 70518-0763 is active and included in the NDC Directory. The product was first marketed by Remedyrepack Inc. on October 06, 2017 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 70518-0763-0?

    The 11-digit format is 70518076300. 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
    5-4-170518-0763-05-4-270518-0763-00