NDC Package 24658-720-01 Flavoxate 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:
24658-720-01
Package Description:
100 TABLET in 1 BOTTLE
Product Code:
Proprietary Name:
Flavoxate Hydrochloride
Non-Proprietary Name:
Flavoxate Hydrochloride
Substance Name:
Flavoxate Hydrochloride
Usage Information:
Flavoxate hydrochloride tablets are indicated for symptomatic relief of dysuria, urgency, nocturia, suprapubic pain, frequency and incontinence as may occur in cystitis, prostatitis, urethritis, urethrocystitis/urethrotrigonitis. Flavoxate hydrochloride tablets are not indicated for definitive treatment, but are compatible with drugs used for the treatment of urinary tract infections.
11-Digit NDC Billing Format:
24658072001
Billing Unit:
EA - Billing unit of "each" is used when the product is dispensed in discreet units.
NDC to RxNorm Crosswalk:
100 EA
NDC to RxNorm Crosswalk:
  • RxCUI: 1095229 - flavoxATE HCl 100 MG Oral Tablet
  • RxCUI: 1095229 - flavoxate hydrochloride 100 MG Oral Tablet
  • Product Type:
    Human Prescription Drug
    Labeler Name:
    Puracap Laboratories Llc Dba Blu Pharmaceuticals
    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):
    Sample Package:
    No
    FDA Application Number:
    ANDA076835
    Marketing Category:
    ANDA - A product marketed under an approved Abbreviated New Drug Application.
    Start Marketing Date:
    12-15-2016
    Listing Expiration Date:
    12-31-2024
    Exclude Flag:
    N

    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 24658-720-01?

    The NDC Packaged Code 24658-720-01 is assigned to a package of 100 tablet in 1 bottle of Flavoxate Hydrochloride, a human prescription drug labeled by Puracap Laboratories Llc Dba Blu Pharmaceuticals. The product's dosage form is tablet and is administered via oral form.

    Is NDC 24658-720 included in the NDC Directory?

    Yes, Flavoxate Hydrochloride with product code 24658-720 is active and included in the NDC Directory. The product was first marketed by Puracap Laboratories Llc Dba Blu Pharmaceuticals on December 15, 2016 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 24658-720-01?

    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 100.

    What is the 11-digit format for NDC 24658-720-01?

    The 11-digit format is 24658072001. 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
    5-3-224658-720-015-4-224658-0720-01