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  5. NDC Package Code: 60505-6221-0 Olopatadine Hydrochloride

NDC Package 60505-6221-0 Olopatadine Hydrochloride

Solution/ Drops Ophthalmic - 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:
60505-6221-0
Package Description:
1 BOTTLE, PLASTIC in 1 CARTON / 5 mL in 1 BOTTLE, PLASTIC
Product Code:
60505-6221
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) twice daily, every 6 to 8 hours, no more than twice 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:
60505622100
NDC to RxNorm Crosswalk:
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):
OLOPATADINE HYDROCHLORIDE 1 mg/mL
Pharmacologic Class(es):
Sample Package:
No
FDA Application Number:
ANDA078350
Marketing Category:
ANDA - A product marketed under an approved Abbreviated New Drug Application.
Start Marketing Date:
10-06-2022
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 60505-6221-0?

The NDC Packaged Code 60505-6221-0 is assigned to a package of 1 bottle, plastic in 1 carton / 5 ml in 1 bottle, plastic 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 60505-6221 included in the NDC Directory?

Yes, Olopatadine Hydrochloride with product code 60505-6221 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, 2025 if the product is not updated or renewed by the manufacturer.

What is the 11-digit format for NDC 60505-6221-0?

The 11-digit format is 60505622100. 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
5-4-160505-6221-05-4-260505-6221-00