NDC Package 49973-301-31 Azo

Urinary Pain Relief 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:
49973-301-31
Package Description:
15 BLISTER PACK in 1 BOX / 2 TABLET in 1 BLISTER PACK
Product Code:
Proprietary Name:
Azo
Non-Proprietary Name:
Urinary Pain Relief
Substance Name:
Phenazopyridine Hydrochloride
Usage Information:
Use Relief from urinary pain, burning, urgency and frequency associated with urinary tract infections.
11-Digit NDC Billing Format:
49973030131
Billing Unit:
EA - Billing unit of "each" is used when the product is dispensed in discreet units.
NDC to RxNorm Crosswalk:
15 EA
NDC to RxNorm Crosswalk:
  • RxCUI: 1094126 - phenazopyridine HCl 95 MG Oral Tablet
  • RxCUI: 1094126 - phenazopyridine hydrochloride 95 MG Oral Tablet
  • RxCUI: 1094192 - Azo Urinary Pain Relief 95 MG Oral Tablet
  • RxCUI: 1094192 - phenazopyridine hydrochloride 95 MG Oral Tablet [Azo Urinary Pain Relief]
  • Product Type:
    Human Otc Drug
    Labeler Name:
    I-health, 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:
    05-24-2012
    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 49973-301-31?

    The NDC Packaged Code 49973-301-31 is assigned to a package of 15 blister pack in 1 box / 2 tablet in 1 blister pack of Azo, a human over the counter drug labeled by I-health, Inc.. The product's dosage form is tablet and is administered via oral form.This product is billed for "EA" each discreet unit and contains an estimated amount of 15 billable units per package.

    Is NDC 49973-301 included in the NDC Directory?

    Yes, Azo with product code 49973-301 is active and included in the NDC Directory. The product was first marketed by I-health, Inc. on May 24, 2012 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 NDC billing unit for package 49973-301-31?

    The contents of this package are billed per "each", products billed on a per each basis are usually products dispensed in discreet units. The calculated billable units for this package is 15.

    What is the 11-digit format for NDC 49973-301-31?

    The 11-digit format is 49973030131. 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
    5-3-249973-301-315-4-249973-0301-31