NDC Package 43598-826-07 Eye Allergy Itch And Redness Relief Twice Daily Relief

Olopatadine Hydrochloride Ophthalmic 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:
43598-826-07
Package Description:
1 BOTTLE, PLASTIC in 1 CARTON / 5 mL in 1 BOTTLE, PLASTIC
Product Code:
Proprietary Name:
Eye Allergy Itch And Redness Relief Twice Daily Relief
Non-Proprietary Name:
Olopatadine Hydrochloride Ophthalmic
Substance Name:
Olopatadine Hydrochloride
Usage Information:
• adults and children 2 years of age and older: • put 1 drop in the affected eye(s) twice daily, every 6 to 8 hours, no more than twice per day • if using other ophthalmic products while using this product, wait at least 5 minutes between each product • replace cap after each use   • children under 2 years of age: consult a doctor
11-Digit NDC Billing Format:
43598082607
NDC to RxNorm Crosswalk:
  • RxCUI: 1111339 - olopatadine HCl 0.1 % Ophthalmic Solution
  • RxCUI: 1111339 - olopatadine 1 MG/ML Ophthalmic Solution
  • RxCUI: 1111339 - olopatadine 0.1 % Ophthalmic Solution
  • RxCUI: 1111339 - olopatadine 1 MG/ML (as olopatadine HCl 1.11 MG/ML) Ophthalmic Solution
  • Product Type:
    Human Otc Drug
    Labeler Name:
    Dr. Reddy's Laboratories Inc.
    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:
    ANDA209619
    Marketing Category:
    ANDA - A product marketed under an approved Abbreviated New Drug Application.
    Start Marketing Date:
    10-01-2020
    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.

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    Frequently Asked Questions

    What is NDC 43598-826-07?

    The NDC Packaged Code 43598-826-07 is assigned to a package of 1 bottle, plastic in 1 carton / 5 ml in 1 bottle, plastic of Eye Allergy Itch And Redness Relief Twice Daily Relief, a human over the counter drug labeled by Dr. Reddy's Laboratories Inc.. The product's dosage form is solution/ drops and is administered via ophthalmic form.

    Is NDC 43598-826 included in the NDC Directory?

    Yes, Eye Allergy Itch And Redness Relief Twice Daily Relief with product code 43598-826 is active and included in the NDC Directory. The product was first marketed by Dr. Reddy's Laboratories Inc. on October 01, 2020 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 43598-826-07?

    The 11-digit format is 43598082607. 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
    5-3-243598-826-075-4-243598-0826-07