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  5. NDC Package Code: 69729-137-14 Pentrexcilina Day Time

NDC Package 69729-137-14 Pentrexcilina Day Time

Cetirizine Hydrochloride Tablet Oral - 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:
69729-137-14
Package Description:
14 TABLET in 1 BOTTLE
Product Code:
69729-137
Proprietary Name:
Pentrexcilina Day Time
Non-Proprietary Name:
Cetirizine Hydrochloride
Substance Name:
Cetirizine Hydrochloride
Usage Information:
Adults & Children 6 years and over One 10mg tablet once daily; do not take more than one 10mg tablet in 24 hours. A 5 mg product may be appropriate for less severe symptoms Adults 65 years and over ask a doctor Children under 6 years ask a doctor Consumers with liver or kidney disease ask a doctor
11-Digit NDC Billing Format:
69729013714
NDC to RxNorm Crosswalk:
Product Type:
Human Otc Drug
Labeler Name:
Opmx Llc
Dosage Form:
Tablet - A solid dosage form containing medicinal substances with or without suitable diluents.
Administration Route(s):
Oral - Administration to or by way of the mouth.
Active Ingredient(s):
CETIRIZINE HYDROCHLORIDE 10 mg/1
Pharmacologic Class(es):
Sample Package:
No
FDA Application Number:
ANDA209274
Marketing Category:
ANDA - A product marketed under an approved Abbreviated New Drug Application.
Start Marketing Date:
11-15-2024
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 69729-137-14?

The NDC Packaged Code 69729-137-14 is assigned to a package of 14 tablet in 1 bottle of Pentrexcilina Day Time, a human over the counter drug labeled by Opmx Llc. The product's dosage form is tablet and is administered via oral form.

Is NDC 69729-137 included in the NDC Directory?

Yes, Pentrexcilina Day Time with product code 69729-137 is active and included in the NDC Directory. The product was first marketed by Opmx Llc on November 15, 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 69729-137-14?

The 11-digit format is 69729013714. 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
5-3-269729-137-145-4-269729-0137-14