NDC Package 80584-113-24 Stix Maximum Strength Urinary Pain Relief

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

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:
80584-113-24
Package Description:
1 BLISTER PACK in 1 CARTON / 24 TABLET in 1 BLISTER PACK
Product Code:
Proprietary Name:
Stix Maximum Strength Urinary Pain Relief
Non-Proprietary Name:
Phenazopyridine Hydrochloride
Substance Name:
Phenazopyridine Hydrochloride
Usage Information:
■ adults and children 12 years and over:take 2 tablets 3 times daily with a full glass of water, with or after meals as needed■ children under 12 years: consult a doctor■ Do not use for more than 2 days (12 tablets) without consulting a doctor
11-Digit NDC Billing Format:
80584011324
NDC to RxNorm Crosswalk:
  • RxCUI: 1094147 - phenazopyridine HCl 99.5 MG Oral Tablet
  • RxCUI: 1094147 - phenazopyridine hydrochloride 99.5 MG Oral Tablet
  • Product Type:
    Human Otc Drug
    Labeler Name:
    Get Stix Inc.
    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.
  • 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:
    09-30-2020
    Listing Expiration Date:
    12-31-2024
    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 80584-113-24?

    The NDC Packaged Code 80584-113-24 is assigned to a package of 1 blister pack in 1 carton / 24 tablet in 1 blister pack of Stix Maximum Strength Urinary Pain Relief, a human over the counter drug labeled by Get Stix Inc.. The product's dosage form is tablet and is administered via oral form.

    Is NDC 80584-113 included in the NDC Directory?

    Yes, Stix Maximum Strength Urinary Pain Relief with product code 80584-113 is active and included in the NDC Directory. The product was first marketed by Get Stix Inc. on September 30, 2020 and its listing in the NDC Directory is set to expire on December 31, 2024 if the product is not updated or renewed by the manufacturer.

    What is the 11-digit format for NDC 80584-113-24?

    The 11-digit format is 80584011324. 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
    5-3-280584-113-245-4-280584-0113-24