NDC Package 60505-6222-2 Olopatadine Hydrochloride

Solution/ Drops Ophthalmic - 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:
60505-6222-2
Package Description:
1 BOTTLE, PLASTIC in 1 CARTON / 2.5 mL in 1 BOTTLE, PLASTIC (60505-6222-1)
Product Code:
Proprietary Name:
Olopatadine Hydrochloride
Non-Proprietary Name:
Olopatadine Hydrochloride
Substance Name:
Olopatadine Hydrochloride
Usage Information:
Adults and children 2 years and older:put 1 drop in the affected eye(s) once daily, no more than once per dayif using other ophthalmic products while using this product, wait at least 5 minutes between each productreplace cap after each usechildren under 2 years of age:Consult a doctor
11-Digit NDC Billing Format:
60505622202
NDC to RxNorm Crosswalk:
  • RxCUI: 1111343 - olopatadine HCl 0.2 % Ophthalmic Solution
  • RxCUI: 1111343 - olopatadine 2 MG/ML Ophthalmic Solution
  • RxCUI: 1111343 - olopatadine 0.2 % Ophthalmic Solution
  • RxCUI: 1111343 - olopatadine 2 MG/ML (as olopatadine HCl 2.22 MG/ML) Ophthalmic Solution
  • Product Type:
    Human Otc Drug
    Labeler Name:
    Apotex Corp.
    Dosage Form:
    Solution/ Drops - A solution which is usually administered in a drop-wise fashion.
    Administration Route(s):
  • Ophthalmic - Administration to the external eye.
  • Active Ingredient(s):
    Sample Package:
    No
    FDA Application Number:
    ANDA090918
    Marketing Category:
    ANDA - A product marketed under an approved Abbreviated New Drug Application.
    Start Marketing Date:
    10-06-2022
    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.

    Other Product Packages

    The following packages are also available for this product:

    NDC Package CodePackage Description
    60505-6222-32 BOTTLE, PLASTIC in 1 CARTON / 2.5 mL in 1 BOTTLE, PLASTIC

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 60505-6222-2?

    The NDC Packaged Code 60505-6222-2 is assigned to a package of 1 bottle, plastic in 1 carton / 2.5 ml in 1 bottle, plastic (60505-6222-1) of Olopatadine Hydrochloride, a human over the counter drug labeled by Apotex Corp.. The product's dosage form is solution/ drops and is administered via ophthalmic form.

    Is NDC 60505-6222 included in the NDC Directory?

    Yes, Olopatadine Hydrochloride with product code 60505-6222 is active and included in the NDC Directory. The product was first marketed by Apotex Corp. on October 06, 2022 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 60505-6222-2?

    The 11-digit format is 60505622202. 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
    5-4-160505-6222-25-4-260505-6222-02