Nuvicare-urinary Pain Relief Maximum Strength Tablet
NDC Package 84324-042-01

View Billable Units, 11-Digit Conversion Format, and RxNorm mappings
Table of Contents
    1. Package Information
    2. Frequently Asked Questions

Package Information

Nuvicare-urinary Pain Relief Maximum Strength (phenazopyridine hydrochloride) tablets is ■ Adults and children 12 years and older: Take 2 tablets 3 times daily with or after meals as needed for up to two days. This formulation utilizes a tablet delivery system. Marketed by Nuvicare Llc, this product is identified by NDC 84324-042.

Identification & Billing

NDC Package Code
84324-042-01
Package Description
1 BLISTER PACK in 1 CARTON / 24 TABLET in 1 BLISTER PACK
Product Code
84324-042
11-Digit Billing Format
84324004201

Clinical Specifications

Proprietary Name
Nuvicare-urinary Pain Relief Maximum Strength
Non-Proprietary Name
Phenazopyridine Hydrochloride
Substance Name
Phenazopyridine Hydrochloride
Dosage Form
Tablet - A solid dosage form containing medicinal substances with or without suitable diluents.
Administration Route
Oral - Administration to or by way of the mouth.
Active Ingredient(s)
PHENAZOPYRIDINE HYDROCHLORIDE 99.5 mg/1
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: Do not use without consulting a doctor.

Regulatory & Marketing

Labeler Name
Nuvicare Llc
Product Type
Human Otc Drug
Marketing Category
UNAPPROVED DRUG OTHER - An unapproved drug product in a marketing category that is not reflected on a particular list.
Start Marketing Date
08-04-2026
Listing Expiration
12-31-2027
Exclude Flag
N
Sample Package
No

Hierarchy Structure

Code Lineage

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 full disclaimer at the bottom of this page.

Frequently Asked Questions

What is the distribution configuration for this product package?

The code 84324-042-01 identifies a specific commercial package of 1 blister pack in 1 carton / 24 tablet in 1 blister pack of Nuvicare-urinary Pain Relief Maximum Strength, a human over the counter drug labeled by Nuvicare Llc. This tablet is formulated for oral use and contains phenazopyridine hydrochloride as the active substance.

Is this product currently listed with the FDA?

Yes, this product is active and verified within the NDC Directory. It was introduced to the market by Nuvicare Llc on August 04, 2026. The current certification is valid through December 31, 2027.

How is this Nuvicare Llc product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 84324004201. The table below illustrates the segment conversion from the 10-digit labeler code to the 11-digit provider format.

11-Digit Code Conversion

Billing payers usually require a 5-4-2 segment configuration. Below is the conversion from the 10-digit package format to the 11-digit billing format:

10-Digit Format (5-3-2)
84324-042-01
11-Digit CMS (5-4-2)
84324-0042-01

Note: The zero is added to the Product segment to maintain the 5-4-2 structure.