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  5. NDC Package Code: 80513-517-72 Maximum Strength Urinary Pain Relief

NDC Package 80513-517-72 Maximum Strength Urinary Pain Relief

Phenazopyridine 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:
80513-517-72
Package Description:
72 TABLET in 1 BOTTLE
Product Code:
80513-517
Proprietary Name:
Maximum Strength Urinary Pain Relief
Non-Proprietary Name:
Phenazopyridine Hydrochloride
Substance Name:
Phenazopyridine Hydrochloride
Usage Information:
• Adults and children 12 years and older:Take 2 tablets 3 times daily with or after meals as needed for up to two days. Take with a full glass of water. Do not use for more than 2 days (12 tablets) without consulting a doctor.• Children under 12 years:Do not use without consulting a doctor
11-Digit NDC Billing Format:
80513051772
NDC to RxNorm Crosswalk:
Product Type:
Human Otc Drug
Labeler Name:
Advanced Rx 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):
PHENAZOPYRIDINE HYDROCHLORIDE 99.5 mg/1
Sample Package:
No
Marketing Category:
UNAPPROVED DRUG OTHER - An unapproved drug product in a marketing category that is not reflected on a particular list.
Start Marketing Date:
05-01-2024
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.

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Frequently Asked Questions

What is NDC 80513-517-72?

The NDC Packaged Code 80513-517-72 is assigned to a package of 72 tablet in 1 bottle of Maximum Strength Urinary Pain Relief, a human over the counter drug labeled by Advanced Rx Llc. The product's dosage form is tablet and is administered via oral form.

Is NDC 80513-517 included in the NDC Directory?

Yes, Maximum Strength Urinary Pain Relief with product code 80513-517 is active and included in the NDC Directory. The product was first marketed by Advanced Rx Llc on May 01, 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 80513-517-72?

The 11-digit format is 80513051772. 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
5-3-280513-517-725-4-280513-0517-72