1. Home
  2. Labeler Index
  3. Glenmark Therapeutics Inc., Usa
  4. 72657-168
  5. NDC Package Code: 72657-168-50 Olopatadine Hydrochloride

NDC Package 72657-168-50 Olopatadine Hydrochloride

Olopatadine Hydrochloride Ophthalmic Solution 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:
72657-168-50
Package Description:
1 BOTTLE, PLASTIC in 1 CARTON / 5 mL in 1 BOTTLE, PLASTIC
Product Code:
72657-168
Proprietary Name:
Olopatadine Hydrochloride
Non-Proprietary Name:
Olopatadine Hydrochloride Ophthalmic
Substance Name:
Olopatadine Hydrochloride
Usage Information:
Usestemporarily relieves itchy and red eyes due to pollen, ragweed, grass, animal hair and dander
11-Digit NDC Billing Format:
72657016850
NDC to RxNorm Crosswalk:
Product Type:
Human Otc Drug
Labeler Name:
Glenmark Therapeutics Inc., Usa
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):
OLOPATADINE HYDROCHLORIDE 1 mg/mL
Pharmacologic Class(es):
Sample Package:
No
FDA Application Number:
ANDA200810
Marketing Category:
ANDA - A product marketed under an approved Abbreviated New Drug Application.
Start Marketing Date:
07-26-2024
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 72657-168-50?

The NDC Packaged Code 72657-168-50 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 Glenmark Therapeutics Inc., Usa. The product's dosage form is solution and is administered via ophthalmic form.

Is NDC 72657-168 included in the NDC Directory?

Yes, Olopatadine Hydrochloride with product code 72657-168 is active and included in the NDC Directory. The product was first marketed by Glenmark Therapeutics Inc., Usa on July 26, 2024 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 72657-168-50?

The 11-digit format is 72657016850. 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
5-3-272657-168-505-4-272657-0168-50