NDC Package 46122-672-64 Olopatadine Hydrochloride

Solution 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:
46122-672-64
Package Description:
1 BOTTLE, PLASTIC in 1 CARTON / 5 mL in 1 BOTTLE, PLASTIC
Product Code:
Proprietary Name:
Olopatadine Hydrochloride
Non-Proprietary Name:
Olopatadine Hydrochloride
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 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:
46122067264
Billing Unit:
ML - Billing unit of "milliliter" is used when a product is measured by its liquid volume.
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:
    Amerisource Bergen
    Dosage Form:
    Solution - A clear, homogeneous liquid1 dosage form that contains one or more chemical substances dissolved in a solvent or mixture of mutually miscible solvents.
    Administration Route(s):
  • Ophthalmic - Administration to the external eye.
  • Active Ingredient(s):
    Sample Package:
    No
    FDA Application Number:
    ANDA204812
    Marketing Category:
    ANDA - A product marketed under an approved Abbreviated New Drug Application.
    Start Marketing Date:
    01-20-2021
    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.

    Frequently Asked Questions

    What is NDC 46122-672-64?

    The NDC Packaged Code 46122-672-64 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 Amerisource Bergen. The product's dosage form is solution and is administered via ophthalmic form.

    Is NDC 46122-672 included in the NDC Directory?

    Yes, Olopatadine Hydrochloride with product code 46122-672 is active and included in the NDC Directory. The product was first marketed by Amerisource Bergen on January 20, 2021 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 NDC billing unit for package 46122-672-64?

    The contents of this package are billed per "ml or milliliter", products billed per milliliter are usually products measured by liquid volume.

    What is the 11-digit format for NDC 46122-672-64?

    The 11-digit format is 46122067264. 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
    5-3-246122-672-645-4-246122-0672-64