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  5. NDC Package Code: 73712-114-12 Uqora Maximum Uti Pain Relief

NDC Package 73712-114-12 Uqora Maximum Uti Pain Relief

Phenazopyridine Hydrochloride Tablet Oral - View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. Other Packages
    3. 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:
73712-114-12
Package Description:
1 BLISTER PACK in 1 CARTON / 12 TABLET in 1 BLISTER PACK
Product Code:
73712-114
Proprietary Name:
Uqora Maximum Uti Pain Relief
Non-Proprietary Name:
Phenazopyridine Hydrochloride
Substance Name:
Phenazopyridine Hydrochloride
11-Digit NDC Billing Format:
73712011412
Product Type:
Human Otc Drug
Labeler Name:
Bonafide Health, Llc Dba Uqora
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:
10-27-2025
Listing Expiration Date:
12-31-2026
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.

Other Product Packages

The following packages are also available for this product:

NDC Package CodePackage Description
73712-114-241 BLISTER PACK in 1 CARTON / 24 TABLET in 1 BLISTER PACK

* Please review the disclaimer below.

Frequently Asked Questions

What is NDC 73712-114-12?

The NDC Packaged Code 73712-114-12 is assigned to a package of 1 blister pack in 1 carton / 12 tablet in 1 blister pack of Uqora Maximum Uti Pain Relief, a human over the counter drug labeled by Bonafide Health, Llc Dba Uqora. The product's dosage form is tablet and is administered via oral form.

Is NDC 73712-114 included in the NDC Directory?

Yes, Uqora Maximum Uti Pain Relief with product code 73712-114 is active and included in the NDC Directory. The product was first marketed by Bonafide Health, Llc Dba Uqora on October 27, 2025 and its listing in the NDC Directory is set to expire on December 31, 2026 if the product is not updated or renewed by the manufacturer.

What is the 11-digit format for NDC 73712-114-12?

The 11-digit format is 73712011412. 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
5-3-273712-114-125-4-273712-0114-12