NDC Package 63187-648-10 Neomycin And Polymyxin B Sulfates And Hydrocortisone

Neomycin Sulfate,Polymyxin B Sulfate And Hydrocortisone Suspension 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:
63187-648-10
Package Description:
10 mL in 1 BOTTLE, PLASTIC
Product Code:
Proprietary Name:
Neomycin And Polymyxin B Sulfates And Hydrocortisone
Non-Proprietary Name:
Neomycin Sulfate, Polymyxin B Sulfate And 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, and for the treatment of infections of mastoidectomy and fenestration cavities caused by organisms susceptible to the antibiotics.
11-Digit NDC Billing Format:
63187064810
NDC to RxNorm Crosswalk:
  • RxCUI: 310687 - hydrocortisone 10 MG (1 % ) / neomycin sulfate 3.5 MG / polymyxin B sulfate 10,000 UNT per mL Otic Suspension
  • RxCUI: 310687 - hydrocortisone 10 MG/ML / neomycin 3.5 MG/ML / polymyxin B 10000 UNT/ML Otic Suspension
  • RxCUI: 310687 - hydrocortisone 10 MG / neomycin 3.5 MG / polymyxin B 10,000 UNT per 1 ML Otic Suspension
  • Product Type:
    Human Prescription Drug
    Labeler Name:
    Proficient Rx Lp
    Dosage Form:
    Suspension - A liquid1 dosage form that contains solid particles dispersed in a liquid vehicle.
    Administration Route(s):
  • Auricular (otic) - Administration to or by way of the ear.
  • Sample Package:
    No
    FDA Application Number:
    ANDA062488
    Marketing Category:
    ANDA - A product marketed under an approved Abbreviated New Drug Application.
    Start Marketing Date:
    03-17-2003
    Listing Expiration Date:
    12-31-2024
    Exclude Flag:
    N

    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 63187-648-10?

    The NDC Packaged Code 63187-648-10 is assigned to a package of 10 ml in 1 bottle, plastic of Neomycin And Polymyxin B Sulfates And Hydrocortisone, a human prescription drug labeled by Proficient Rx Lp. The product's dosage form is suspension and is administered via auricular (otic) form.

    Is NDC 63187-648 included in the NDC Directory?

    Yes, Neomycin And Polymyxin B Sulfates And Hydrocortisone with product code 63187-648 is active and included in the NDC Directory. The product was first marketed by Proficient Rx Lp on March 17, 2003 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 63187-648-10?

    The 11-digit format is 63187064810. 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
    5-3-263187-648-105-4-263187-0648-10